On 2025-04-15 15:24:19, user Mohieddin Jafari wrote:
This manuscript was published in Proteomics Journal at the following link and the link has not appeared on this page yet after 4 weeks: https://analyticalsciencejournals.onlinelibrary.wiley.com/doi/full/10.1002/pmic.202400238
On 2025-04-15 13:14:47, user Donald R. Forsdyke wrote:
THE "ACCENT" OF DNA
You can explain the "de-extinction" problem, be it with mice or dire wolf, historically by considering the four bases in DNA sequences:
Chargaff circa 1950 discovered that DNA base composition (not sequence) was a species characteristic, simply expressed as GC% (as opposed to AT%).
So, there were GC%-rich species and AT%-rich species, with the exact values differing between species.
We biochemists and others discovered circa 1990 that actually the difference was due to short sequences (k-mers).
Thus, for k=3. GC%-rich species would be enriched in GTC, GGA, GGC, CAG, etc. Whereas for an AT-rich species ACT, AAG, AAT, TGA, etc.
Given 4 bases (A, C, G, T), for k=2 there would be 4x4 = 16 possibilities. For k=3 there would be 4x4x4 = 64 possibilities.
In practice the range varies from k=3 to k=8.
Fragments of DNA from, say, a soil sample, will correspond to a variety of species in the sample. But just by assessing the k-mer patterns in the fragments, those corresponding to each species can be identified.
Then you can look at the fragments corresponding to one species and examine long sections to identify gene sequences (viewed as "sentences" or "word strings").
So, k-mers can be seen as the "accent" or "dialect" of DNA that relates to what species it belongs to. Unless you take that into account you cannot make a new species by just inserting a few genes to change appearance.
Just as accent can influence reproductive choices between humans (remember Eliza Doolittle), so it influences the reproductive isolation that is the defining characteristic of a species.
[A paper in the December 2024 issue of the Journal of Theoretical Biology goes into more details. Or see my textbook - Evolutionary Bioinformatics (3rd edition, 2016).]
On 2025-04-15 13:10:09, user Donald R. Forsdyke wrote:
THE "ACCENT" OF DNA
You can explain the "de-extinction" problem, be it mice or dire wolf, historically by considering the four bases in DNA sequences:
Chargaff circa 1950 discovered that DNA base composition (not sequence) was a species characteristic, simply expressed as GC% (as opposed to AT%).
So, there were GC%-rich species and AT%-rich species, with the exact values differing between species.
We biochemists and others discovered circa 1990 that actually the difference was due to short sequences (k-mers).
Thus, for k=3. GC%-rich species would be enriched in GTC, GGA, GGC, CAG, etc. Whereas for an AT-rich species ACT, AAG, AAT, TGA, etc.
Given 4 bases (A, C, G, T), for k=2 there would be 4x4 = 16 possibilities. For k=3 there would be 4x4x4 = 64 possibilities.
In practice the range varies from k=3 to k=8.
Fragments of DNA from, say, a soil sample, will correspond to a variety of species in the sample. But just by assessing the k-mer patterns in the fragments, those corresponding to each species can be identified.
Then you can look at the fragments corresponding to one species and examine long sections to identify gene sequences (viewed as "sentences" or "word strings").
So, k-mers can be seen as the "accent" or "dialect" of DNA that relates to what species it belongs to. Unless you take that into account you cannot make a new species by just inserting a few genes to change appearance.
Just as accent can influence reproductive choices between humans (remember Eliza Doolittle), so it influences the reproductive isolation that is the defining characteristic of a species.
[A paper in the December 2024 issue of the Journal of Theoretical Biology goes into more details. Or see my textbook - Evolutionary Bioinformatics (3rd edition, 2016).]
On 2025-03-05 19:55:42, user Enrico Radaelli wrote:
In this viral video on YouTube<br /> https://www.youtube.com/watch?v=WNuzopVDFQs <br /> The company claims that "There were no unintended consequences except adorability".<br /> However, the mice are clearly pruritic and they exhibit crusty/flaky skin in glabrous areas (especially paws and eyelids).<br /> I wonder if this is part of the phenotype or if the mice contracted infections that might have caused these lesions (mites, C. bovis, etc.).
On 2025-04-15 13:02:01, user Kai Dallmeier wrote:
Article has in the meantime been published as:
Degryse J, Maas E, Lassaunière R, Geerts K, Kumpanenko Y, Weynand B, Maes P, Neyts J, Thibaut HJ, Alpizar YA, Dallmeier K. Antigenic Imprinting Dominates Humoral Responses to New Variants of SARS-CoV-2 in a Hamster Model of COVID-19. Microorganisms. 2024 Dec 14;12(12):2591. doi: 10.3390/microorganisms12122591. PMID: 39770793; PMCID: PMC11678355.
On 2025-04-15 10:58:18, user ryhisner wrote:
This is amazing. Thank you so much for this work. The paper tantalizingly mentions more detailed images of the structure in supplemental figures, but they are not included in the PDF and do not seem to be available for download. Will they be posted soon?
Also, is there any chance your Alphafold models (and manual extension of the model to the full pp1a’-nsp4-nsp10 + pp1ab’-nsp4-nsp16) can be made available for others to view? I'm very interested in the proximity of specific AA residues throughout the complex, which may help explain unusual mutational patterns throughout the replicase complex that have emerged independently hundreds of times.
On 2025-04-15 00:40:23, user Gennady Gorin wrote:
Will the GitHub repository be made public?
On 2025-04-14 12:53:05, user Cedar wrote:
On 2025-04-14 00:54:09, user Capra internetensis wrote:
Are you planning to analyze the Y chromosomes? There is a severe shortage of high-resolution Y chromosomal data from Australia, and patrilines often show very different patterns from matrilines.
On 2025-04-13 06:29:39, user Jianshu Zhao wrote:
Dear PanSpace authors, thank you for this excellent work! I have a few questions related to the benchmark. The comparison between PanSpace and GSearch for space requirement is not clear to me because it says very clear in the abstract of GSearch paper that, it only requires 2.5G space using the SetSketch option, which is around 6G only for AllThebacteria, but not 80G for the default ProbMinHash option. ProbMinHash is very space inefficient since it considered all kmers and their abundance while SetSketch is very space efficient and also fast (not so fast as the fastest option Densified MinHash). Also, for genus level classification, GSearch can be done in amino acid space (after predicting genes), which ANI in nt space will lose accuracy (a well know problem). Can the genus level benchmark be done also in amino acid space, which is also clearly there in abstract (3-step framework). Thanks! Jianshu
On 2025-04-12 02:40:33, user Julian C wrote:
To appear in J Prot Res (accepted April 11, 2025).
On 2025-04-11 15:45:59, user Alizée Malnoë wrote:
The manuscript by Azulay et al. investigates the cooperative interaction between Listeria monocytogenes (Lm) strain 10403S and its prophage ɸ10403S. The authors identify and characterize a novel anti-phage defense system that is encoded in the genome of the prophage focusing on the ORF65 protein renamed TerI (for terminase inhibitor). The study shows that TerI inhibits phage reproduction by targeting the phage terminase complex of invading phages, thus preventing the packaging of phage DNA. Azulay et al. also discover two other prophage encoded proteins that provide the phage with immunity against its own TerI protein and thus enable packaging of its own genetic material. This preprint is well-written and contains high-quality data that advances the field of phage biology and anti-phage defense systems. We provide below some suggestions to strengthen the methodology, and to increase the clarity in the interpretation of the results.
Major comments<br /> A loading control is required in Figure 1B, 2F, 2G, and 4D to verify that the amount of protein entered into each well is the same either using an antibody against a protein that does not change or using Coomassie or Ponceau stain of the membrane. Additionally, relative quantification (to the loading control) of immunoblots would be helpful to measure the loss of ORF65 co-sedimentation in the ΔterSL mutant (Figure 2G) to strengthen the finding that ORF65/TerI interacts with TerS. For Figure 2F, a quantification of the immunoblot, ideally including a dilution series, would further support the statement that both the bacterial strains, expressing ORF65 or not, produced or released a similar number of capsids.
Page 11: “ectopic expression of each of these genes alone (i.e., without TerI expression) did not affect virion production, as compared to WT bacteria, suggesting that the encoded proteins play a specific role in neutralizing TerI.” In Figure 3D, the ectopic expression of LMRG_01518 shows a large standard deviation reaching about 50%WT in PFU, suggesting that overexpression of LMRG_01518 may impact virion production. We recommend showing individual data points of each replicate and to provide a possible explanation for this high standard deviation.
Page 12: “Altogether, these findings indicated that TerI is fully active during 10403S induction and that LMRG_01518 and LMRG_02984 counteract its activity, functioning as self-immunity proteins that allow 10403S DNA packaging and virion assembly”. However, only LMRG_02984 directly interacts with TerI and not LMRG_01518 (Figure 3H). This data may explain the stronger phage ɸ10403S rescue consistently observed when LMRG_02984 is present compared to LMRG_01518 (Figure 3E). There is a question as to whether the results, as currently reported, fully support the direct interaction of LMRG_01518 with TerI. The study could incorporate a BACTH assay between LMRG_02984 and LMRG_01518 to support that conclusion, or the text could be revised to ensure the conclusions tightly align to the findings currently included (e.g. the model in Figure 5 depicts direct interaction between anti-TerI1(01518) and TerI).
The discussion, while well-written, reads more like a minireview and could focus more on the findings. It could be expanded by elaborating more on the data presented and how it supports the model presented in Figure 5. Of particular interest is the discussion of LMRG_01518 inhibiting TerI function although not interacting with TerI directly. Other interesting points to discuss include the specificity of the TerI/anti-TerI1, I2 system, could the invading phage encode anti-TerI as well? How about the TerI/TerS specificity, from the data presented, it seems that TerI is able to inhibit TerS from different phages. Is there anything known about the function of LMRG_01518 and LMRG_02984 besides their role as anti-TerI? On Figure 3C, it seems that expression of LMRG_01517 largely decreases PFU compared to control, this result could be discussed.
We realize it is beyond the scope of this study, but it would be of interest to perform a BLAST search with terI. This novel anti-phage defense system might be used by other temperate phages in other bacteria. It would be interesting to see how many other phages use this system. Or perhaps this is something exclusive to the Lm phages?
Minor comments<br /> - Page 6: could you explain the choice of not using the his-tagged ORF65 from Figure 1E and on. We understand this may be technically difficult due to lack of specific antibodies against TerI and anti-TerI1 and 2, but something that was not obvious to us was whether the ectopic expression of ORF65 resulted in overexpression compared to endogenous levels in WT and whether exogenous infection leads to anti-terI1 and anti-terI2 expression. Figure 1F, we would have expected higher PFU than WT in the ATG*orf65 if ORF65 is present in WT to prevent virion production, and Figure 1G, we would have expected some level of PFU if anti-TerI are present to counteract TerI.<br /> There is a sentence that could be clarified “To this end, we infected Lm bacteria cured of ɸ10403S and deleted the comKgene with free particles of ɸ10403S in the presence or absence of orf65 ectopic expression (i.e…).” Consider breaking it into two: “We made ΔcomK Lm bacteria cured of ɸ10403S (Lm Δɸ10403S-ΔcomK). We then infected Lm Δɸ10403S-ΔcomK with ɸ10403S particles in the presence or absence of orf65 ectopic expression…”<br /> - Page 11: could you clarify the following sentence “cro (corresponding to the first early gene)” and define the acronym cro in the first instance. It is not clear to us whether cro itself is considered an early gene as it represses early genes.<br /> - Methods: could you describe how the ATG*orf65 mutation was exactly made and explain the choice of this mutation as opposed to deleting the Shine-Dalgarno sequence of the rpsD promoter (if it contains one). Could you also explain why the mutagenesis of the -10 box of the orf65 promoter involved 5 bases and not less.<br /> - Figure 1A (and 3A): LMRG_01515 is labeled as LMRG_1515, include the missing zero in the locus number.<br /> - Figure 1C, 1E, 2C, 2D: plot growth curves on a log scale rather than linear as it is standard in the field.<br /> - Figure 1F, 3C, 3D: y-axis of PFU (% WT) needs to be consistent and should be put on a linear scale rather than a logarithmic scale as it is standard in the field. Provide number of replicates in the panel (such as N = 3).<br /> - Figure 1H: clarify which ones are lytic or temperate (prophages) in the panel by adding labels below the phage names. Also, keep consistent the nomenclature of the phages in the text to match figures (phage names missing phi symbol in text).<br /> - Figure 2F: could you explain the choice of quantifying attP rather than attB.<br /> - Figure 2E: increase scale size and keep panel sizes consistent and aligned.<br /> - Figure 2G: explain the low level of ORF65 detected in the ΔΦ pellet in the first panel. Are the ΔterS and ΔterL mutants available, it would be of interest to test these as well to strengthen the BACTH assay in Figure 2H showing direct interaction with TerS but not L. This may be technically challenging, but all samples could be run on one gel to produce one blot, if possible, for ease of comparison. <br /> - Figure 3: for consistency in the panels presented, the nomenclature used to describe LMRG_02984 and LMRG_01518 should not be changed to anti-TerI1 and anti-TerI2.<br /> - Figure 3A: make the phage genome image larger and include description in the legend.<br /> - Figure 3H: LMRG_01518 was included as part of the negative controls.
Maddy McPherson and Octavio Origel (Indiana University Bloomington) - not prompted by a journal; this review was written within a Peer Review in Life Sciences graduate course led by Alizée Malnoë with input from group discussion including Sally Abulaila, Kim Kissoon, Michael Kwakye, Madison McReynolds, Mandkhai Molomjamts, Habib Ogunyemi and Ren Wilson.
On 2025-04-11 10:18:57, user Bacillus Biofilms wrote:
Now published in Communications Biology https://doi.org/10.1038/s42003-025-07712-w
On 2025-04-11 00:43:55, user Lingyuxiu Zhong wrote:
Sorry to bother you. I hope this comment reaches you well.<br /> I’m currently using your paper for pharmacodynamic data generation and comparison.<br /> I would like to use the MIC value of colistin against the bacteria described in your study.<br /> However, I couldn’t find the specific MIC value in the paper.<br /> May I kindly ask if you could share the exact value with me?
On 2025-04-10 15:36:13, user Mehadi Hasan wrote:
DAssemble combines multiple models to leverage their collective strengths, offers a promising solution to address these issues by improving both performance and interpretability. This can be a breakthrough tool/model in Omics research. All the best to Dr. Himel Mallick and the team.
On 2025-04-10 12:53:55, user Huiwang Ai wrote:
I think the authors just don't understand computational protein design. RFdiffusion is used to generate the shape of the binder, not sequences. You then need other follow-up computational tools.
On 2025-02-12 01:34:43, user Ddeadpanscience wrote:
I think normally rfdiffusion will require that you test at least 48 or 96 designs. The success rate is not that high
On 2025-04-09 23:14:51, user Tasneem Qaqorh wrote:
This has been peer reviewed <br /> Tasneem Qaqorh et al.,Atf3 controls transitioning in female mitochondrial cardiomyopathy as identified by spatial and single-cell transcriptomics.Sci. Adv.11,eadq1575(2025).DOI:10.1126/sciadv.adq1575
On 2025-04-09 16:12:39, user Jana Knoppova wrote:
Ad Extended Fig 1:<br /> There is a BN PAGE band assignated as NDH1-PSI supercomplex, however, I cannot see any results here verifying that it is really so. Could you pls show any verification of this statement.<br /> Thanks, Jana
On 2025-04-09 12:12:39, user Pieter van der velden wrote:
this paper is published in Human Mutation 2020 Dec;41(12):2205-2216. PMID: 32906203<br /> Please add a link to this bioRxiv manuscript.
On 2025-04-08 16:20:46, user Evan Ernst wrote:
Published April 1, 2025 in Current Biology: https://doi.org/10.1016/j.cub.2025.03.013
On 2025-04-08 12:36:14, user MM wrote:
Tracking changes in phenotype over thousands of years is an ambitious endeavour. However, it should be noted that the relationship between genotype and phenotype isn’t fully understood. Also, we know from other ancient DNA studies that the derived alleles in genes SLC24A5 and SLC45A2 associated with light skin pigmentation in Europeans today were either fixed or at high frequency in the Neolithic Anatolian population. Previous studies have linked the introduction of light skin in western, central and southern Europe as coming with the Neolithic Anatolian farmers. Eastern hunter-gatherers seem to have carried these alleles already, so Eastern Europe and Scandinavia followed a different trend. Your method predicted darker skin in the Neolithic Anatolians based on genomes that have already been published, which contradicts the original research, but you ignored this in your paper. The earlier findings need to be taken into consideration here - why does your method contradict these findings? And if you deem your method superior, then how and when did these alleles get introduced in western/southern Europe if it wasn’t with the Anatolian farmers? And why did your method predict darker skin pigmentation in this population when they carried the same derived alleles as modern Europeans?
On 2025-04-07 06:10:36, user Kehinde wrote:
A good and informative study. But I hope you guys are ready for the amount of push back you're going to get because of it.
On 2025-02-25 20:42:31, user Victor Gonzalez Perdomo wrote:
This study seems biased, there is very little data from the Paleolithic, you have data mostly around Neolithic. Also it seems that you have very little ancient data around the southeast Europe. You neither aproach the fact most light pigmentation features appeared close to the atlantic coast then seems to spred to the interior.
On 2025-04-08 11:01:59, user Bob Blasdel Reuter wrote:
What a fantastic manuscript. I have a methodological question though, unless I am missing something, you don’t seem to describe any experiments validating that the radionuclide actually attached to and labelled the phage, or what impact the radiolabel might have on the function and thus structure of the labelled phages.
* Do you have a sense of what fraction of the mCi of I-125 that were injected into each mouse was labelled onto a phage?
* Do you have a sense of how much each labelled phage particle was structurally altered by the labelling? For example, how many particles of the Sulfo-SHPP linker were attached to each phage, and what chemical impact the labelling might have had on labelled phage?
On 2025-04-08 08:47:58, user Yuan Tian wrote:
Interesting! Similar observation with our research!
On 2025-04-08 08:01:47, user Ruoheng Li wrote:
Hi! I noticed that Fig 4D and E axis labels read 'somite width' while the figure legend says 'somite length'.
On 2025-04-08 06:50:41, user Zach Hensel wrote:
Here's a correction for one typo in the manuscript:
Most previous analyses considered datasets in which there was only one A24325G sequence collected prior to 15-Feb-2020 ~~with~~without a market link: a sequence collected in California, USA on 12-Feb-2020 (CA-CDC-8).
This will be updated for future revisions.
On 2025-04-07 16:29:49, user Eduard Porta wrote:
The paper is now published in a peer-reviewed journal:
https://www.cell.com/cell-reports/fulltext/S2211-1247(24)01580-8
On 2025-04-05 21:03:30, user Roy wrote:
now published in :<br /> https://www.mdpi.com/3252542
On 2025-04-05 10:14:49, user Alexis Gautreau wrote:
Dear Dr. Krause,
I would like to draw your attention to an oversight. You forgot to cite a paper from my group, which also reports that NHSL3 regulates cell migration and that NHSL3 interacts with the partners you are also studying: the WAVE complex and Ena/VASP proteins. Our paper by Novikov et al. was published three months ago in Nat Commun:<br /> https://www.nature.com/articles/s41467-024-55647-3
Best regards,
Alexis Gautreau
On 2025-04-04 14:55:40, user Roy Moscona wrote:
This pre-print is not published at :
https://link.springer.com/article/10.1007/s11033-025-10470-x
Under a slightly different name
On 2025-04-04 14:34:39, user Victor Corces wrote:
It's possible that H3K9me3 and H3K27me3 are acting through changes in DNA methylation. It would be interesting to check
On 2025-04-04 13:16:05, user Eva-Maria Geigl wrote:
We agree with the conclusion that the Bell Beaker groups formed locally in (north)western Europe. We proposed last year a similar model in our Science Advances article “Parasayan, O., Laurelut, C., Bole, C., Bonnabel, L., Corona, A., Domenech-Jaulneau, C., Paresys, C., Richard, I., Grange, T., Geigl, E.-M. (2024) Late Neolithic collective burial reveals admixture dynamics during the third millennium BCE and the shaping of the European genome Sci. Adv. 10, eadl2468 (2024). Doi: 10.1126/sciadv.adl2468”. We proposed local formation of Bell Beaker groups in northern France starting ~2600 BCE in a Late Neolithic archaeological context (“Néolithique récent”, formerly called SOM, comprising in its final stage a few dispersed AOC burials) as a result of the merging of (1) north-western CW-associated steppe-ancestry carriers (corresponding to two of your Vlaardingen/CW individuals), (2) individuals associated with the “Néolithique récent” and (3) individuals associated with Maritime Bell Beakers originating from southwestern Europe, the latter two lacking steppe-ancestry. A discussion of our model and a citation of our article is missing in the present manuscript given the similarity of the conclusions drawn herein.
On 2025-04-03 14:25:20, user Jorge Hernández wrote:
This has now been published in PNAS:<br /> https://www.pnas.org/doi/10.1073/pnas.2501915122
On 2025-04-03 12:27:27, user Brian Plosky wrote:
Published in 2020 as https://doi.org/10.1038/s43018-020-0028-4
On 2025-04-03 11:46:02, user Schoolenberg, Machteld wrote:
Dear authors, really nice paper, pleasure to read. I'll use it for my current NFF project on pathways towards the GBF targets. I missed an important, additional reference though, which is the IPBES, 2023 document on zenodo. https://zenodo.org/records/8171339 It is an IPBES document, with the plenary approved description of the NFF and it's official figure (which has been modified since Pereira 2020) as well as a 1st version methodological guidance on using the NFF.<br /> I especially wanted to point out this reference, since your figure 5 is graphically so extremely similar to the approved NFF figure, but without reference to this document. That is either a coincidence, in which case to avoid confusion I'd suggest seeing how to make the two more dissimilar since conceptually they are different. Or on purpose, in which case I think adding 'adapted from IPBES, 2023' is appropriate.<br /> Happy to discuss if needed.<br /> Best wishes, Machteld
On 2025-04-02 17:03:58, user Arval wrote:
This paper has now since been published. Link at: https://doi.org/10.1128/mbio.03428-23
On 2025-04-02 13:38:57, user Prof. T. K. Wood wrote:
Persisters probably do allow for CRISPR adaptation, but this work has nothing to do with persisters since Fig. 1 shows cells are simply dying and never reach anything like a plateau. So another interpretation is that dying cells increase CRISPR adaptation.
On 2025-04-02 09:06:04, user Lee Berger wrote:
On 2025-04-02 09:05:27, user Lee Berger wrote:
On 2025-04-02 09:04:49, user Lee Berger wrote:
On 2025-04-02 08:59:43, user Lee Berger wrote:
On 2025-04-02 08:59:13, user Lee Berger wrote:
On 2025-04-01 17:52:03, user Mathurin Dorel wrote:
Published as https://link.springer.com/article/10.1186/s13046-024-03075-y
On 2025-04-01 15:53:37, user Analabha Roy wrote:
Authors' Note: This preprint was thoroughly rewritten (including the title) after submission for review. The revised version was published in SciRep: Bagchi et. al. A multifaceted examination of the action of PDE4 inhibitor rolipram on MMP2/9 reveals therapeutic implications. Sci Rep 15, 10963 (2025). DOI: 10.1038/s41598-025-95549-y
On 2025-04-01 15:31:09, user Shawn Hurst wrote:
Two points which strengthen your argument are 1) we see socio-emotional differences in great apes, showing different emotional evolution trajectories are possible in hominids despite similar brain sizes, and 2) orbitofrontal cortex is very important for socio-emotional behavior and control- and relative orbitofrontal cortex expansion and reorganization is easy to compare in both living great apes and fossil hominin endocasts, where lateral OFC is smallest in orangutans, appears inflated in A. sediba relative to African apes, and appears similar in relative size between Homo naledi and Homo sapiens.
On 2025-03-31 18:29:21, user Christian Schürings wrote:
This paper has been published now in Ecological Processes:<br /> https://doi.org/10.1186/s13717-025-00593-1
On 2025-03-31 16:09:17, user Michael wrote:
Hi, I'm an author. This has been published in Nature Plants https://www.nature.com/articles/s41477-024-01738-4
On 2025-03-31 14:46:25, user Neelesh Patra wrote:
Published in Plant Physiology and Biochemistry<br /> Volume 222, May 2025, 109679 with DOI: https://doi.org/10.1016/j.plaphy.2025.109679
On 2025-03-31 12:37:24, user Kshitish Acharya wrote:
Our observations from a detailed, quantitative comparisons of pathway databases can help scientists make rational choices among a plethora of options!
On 2025-03-31 09:48:48, user Stephen Thorpe wrote:
This article appears to omit citation and discussion of Rotating coherent scattering microscopy (ROCS) from Alexander Rohrbach's group apart from a brief mention in the methods section. This is highly relevant to this manuscript.
On 2025-03-30 17:03:43, user Evan Saitta wrote:
Currently undergoing major revisions. Advisable to wait until final draft is published before citing.
On 2025-03-30 13:00:42, user MicroDude wrote:
May I suggest a look at https://pubmed.ncbi.nlm.nih.gov/34832944/ (though I can see that the published version of this came out about the published version of this preprint came out about the same time as the recommended article; must have been in the air!)
On 2025-03-28 22:11:44, user Carmen Nieves wrote:
Say prototaxites is something that came from mud or volcanic ash sludge from water- could it be..instead of the whole tadpole/ (frogs)..it could be the slime that these creatures use.. I'm so curious.. ???? .. maybe the beginnings of even jellyfish?? Old coral?
On 2025-03-28 18:03:10, user MicroDude wrote:
Hi, I'm noticing that this reference does not seem to be cited here: https://www.sciencedirect.com/science/article/pii/S0167701211003952
I'm also noticing a lack of referencing to my/our own antibiotic-mediated antagonism of phage infection activities:<br /> https://www.mdpi.com/2079-6382/8/4/182
On 2025-03-28 10:09:01, user Michael Kuhn wrote:
This preprint has now been published: https://www.nature.com/articles/s41586-024-08222-1
On 2025-03-27 21:21:39, user Jeremy Jones wrote:
The methodology presented in this paper is obscure and outdated. Mechanistic modeling is the by far preferred method of choice for translating in silico models to in vivo PK predictions (like the HTPK module in ADMET Predictor). <br /> Furthermore, the actual performance characteristics of all ADMET Predictor models are publicly available and are generally poorly represented by the limited datasets tested in this manuscript.
On 2025-03-27 18:10:43, user Luciano Marcon wrote:
I would like to respectfully point out a misrepresentation regarding our work cited as reference [16] (Raspopovic et al., 2014).
In your manuscript, you write:<br /> “In contrast, many studies with realistic biological geometries either neglect growth or fail to explore how growth rate influences the emergence of patterns [16, 20, 21, 22].”
However, this characterization does not accurately reflect our study. In Raspopovic et al. (2014), we explicitly analyzed the influence of growth on pattern formation, as shown in Figure 3A and Figure 23 of the supplementary data. This analysis was based on a limb growth model derived from experimental clonal data (see also Marcon et al., 2011), and understanding how growth modulates pattern emergence was one of the central aims of that work.
We kindly ask you to consider correcting this point to more accurately reflect the content and focus of our study.
On 2025-03-27 14:41:07, user Mark Price wrote:
A revised version of this paper has been published in IEEE/ASME Transactions on Mechatronics under the title "Design and Characterization of the AdjuSST: An Adjustable Surface Stiffness Treadmill".
On 2025-03-26 20:06:47, user Peng Xu wrote:
It has been published at Science Advances: https://www.science.org/doi/10.1126/sciadv.ads6021
On 2025-03-26 11:31:40, user Chris Bakal wrote:
Many familiar ideas...
On 2025-03-26 10:13:54, user Julia wrote:
This article has been published:<br /> https://www.ahajournals.org/doi/10.1161/CIRCULATIONAHA.123.066961
On 2025-03-26 08:51:39, user Shigeaki Saitoh wrote:
The revised version of this article is published in Journal of Cell Science ( https://doi.org/10.1242/jcs.263747 ).
On 2025-03-25 19:00:15, user Ester Russo wrote:
Hello, authors. I invite you to access our review at the following link: https://prereview.org/reviews/15083524
On 2025-03-25 16:52:28, user Wolf Huetteroth wrote:
Paper published now in Current Biology:<br /> https://www.cell.com/current-biology/fulltext/S0960-9822(25)00055-7
On 2025-03-25 16:50:00, user Deborah Caldeira Brandt Almeid wrote:
This review resulted from the graduate-level course "How to Read and Evaluate Scientific Papers and Preprints" from the University of São Paulo, which aimed to provide students with the opportunity to review scientific articles, develop critical and constructive discussions on the endless frontiers of knowledge, and understand the peer review process.
The work is of great relevance in the field of extracellular vesicles (EVs), as it explores the role of the SUMO (Small Ubiquitin-like Modifier) pathway in the packaging of post-translational proteins in these structures. The data corroborate other studies that seek to understand the packaging mechanisms of extracellular vesicles that can influence the function of vesicles and, consequently, their interaction with target cells, such as in astrocytes, enriching the knowledge of how these pathways are involved in the construction of EVs and modifications, in this case protein modifications.<br /> One detail that caught my attention was the terms used and I would like to comment on a few things: Extracellular vesicles are complex structures that carry information in cellular communication, being responsible for the exchange of molecules between cells, including proteins, lipids, and genetic material. Their function in cellular communication depends on the specific composition of each vesicle, which can vary depending on the type of cell that releases it, for example in the modulation of biological processes, such as the immune response. In addition, the field of study with EV is being increasingly explored, precisely because these small structures are mediators in such important functions in target cells 1,2. However, it is still an area that is expanding and many terms, nomenclatures, and methodologies are still being discussed. Therefore, the use of more general terms involving location, group, and nomenclatures can be strategic to avoid having data invalidated in the future. For example, today the nomenclature “microvesicles” has been invalidated, “exosomes” discouraged and “extracellular vesicles” is well accepted according to MISEV (Minimal Information for Studies of Extracellular Vesicles)3. Another suggestion is to be cautious when declaring the position of the components of these structures if there is no data presented that confirms whether it is inside, on the surface or if it is transmembrane in these released structures. I suggest that the authors perform an assay that really shows the location of the protein.<br /> The viability data should be presented in a graph to support the integrity of the extracellular vesicles obtained. Another control that I believe should be incorporated is the graph of the populations (size and quantity) by NTA obtained from a portion of the sample of extracellular vesicles used in the functional assay, with the corresponding results. Thus, the quantity of extracellular vesicles used can be calculated and also corroborates that the quantity of vesicles does not interfere with the effect on astrocytes, but rather on the proteins involved in SUMOylation.<br /> Finally, when performing functional assays with extracellular vesicles, it is important to incorporate rigorous controls to validate the results. The viability of the cells subjected to vesiculation can also be assessed using rezasurin, and data on the size and quantity of EVs can be presented using NTA (Nanoparticle Tracking Analysis) graphs to ensure that the samples used in the functional assays followed a methodology for good purification and preservation of the integrity of these vesicles. Since storage at -80°C can compromise the bilayer of the EV membrane, the results obtained for size and quantity may change, as well as the form of communication with the target cell of the assay. Immunofluorescence assays can complement the data and elucidate how these EVs interact with the target cell: membrane-membrane contact, fusion between membranes or internalization of these structures. These controls will allow a more accurate assessment of EV functionality and contribute to the understanding of their mechanisms of action. In addition, they can also open new research possibilities, such as the evaluation of the impact of EVs formed by the SUMO pathway in neurodegenerative diseases, such as Alzheimer's, where cellular communication and protein accumulation play key roles in disease progression. Studies in the literature mention disease progression related to the accumulation of beta-amyloid protein and other factors still under investigation, such as changes in the protein profile and receptors of microglia.<br /> Congratulations on your work! Here are some works that may be of interest to the group.<br /> 1. The biology and function of extracellular vesicles in immune response and immunity<br /> Immunity, Volume 57, Issue 8, 1752 - 1768<br /> 2. Challenges and directions in the study of cell-cell communication by extracellular vesicles.<br /> 3. Nat Rev Mol Cell Biol, doi: 10.1038/s41580-022-00460-3 (2022)<br /> 4. Welsh JA, et al. Minimal information for studies of extracellular vesicles (MISEV2023): From basic to advanced approaches. J Extracell Vesicles. doi: 10.1002/jev2.12451. <br /> 5. Exploiting the biogenesis of extracellular vesicles for bioengineering and therapeutic cargo loading. doi: 10.1016/j.ymthe.2023.02.013. <br /> 6. Anti-inflammatory clearance of amyloid-β by a chimeric Gas6 fusion protein. doi: 10.1038/s41591-022-01926-9.
On 2025-03-25 14:23:39, user JANNE MARKUS TOIVONEN wrote:
I would like the authours to double check the statement that "RPL3L ribosomes associate with mitochondria". As far as I have understood it is the opposite, ribosomes with RPL3 associate with mitochondria in RPL3L knockouts.
On 2025-03-24 20:40:02, user Sara, Rosangela e Lucas wrote:
This review resulted from the graduate-level course "How to Read and Evaluate<br /> Scientific Papers and Preprints" from the University of São Paulo, which aimed<br /> to provide students with the opportunity to review scientific articles, develop<br /> critical and constructive discussions on the endless frontiers of knowledge, and<br /> understand the peer review process.<br /> DHRS7 Integrates NADP+ 1 /NADPH Redox Sensing with Inflammatory Li2 pid<br /> Signalling via the Oxoeicosanoid Pathway<br /> Yanan Ma1 , King Lam Hui1 , Yohannes A. Ambaw1 , Tobias C. Walther1,3 3 ,<br /> Robert V. Farese, Jr1 , Miklos Lengyel1 , Zaza Gelashvili1,2 , Dajun Lu1 , and<br /> Philipp Niethammer1,4<br /> Reviewer Team: Lucas Athayde, Rosangela Silva Santos, Sara Ventura.<br /> Summary<br /> Employing a variety of methodological approaches including structural modeling,<br /> phylogenetics, gene silencing, and mass spectrometry, the authors investigate 5-<br /> HEDH activity in A549 cells, an enzyme associated with lipid dehydrogenation<br /> that leads to 5-KETE formation. After confirming 5-HEDH activity through<br /> detection of its reversible oxidation products, 5-KETE and 5-HETE, the study<br /> proceeds with a gene-level investigation and screening for potential microsomal<br /> dehydrogenases involved in this lipid peroxidation. Additionally, the authors<br /> provide insights that may extend to other types of cells, as evidenced by<br /> functional studies in zebrafish.<br /> The authors uncover the role of DHRS7 in redox signaling, demonstrating its<br /> NADPH-dependent regulation of 5-KETE production. Unlike classical redox<br /> signaling based on thiol oxidation, they present DHRS7 as a redox-regulated<br /> enzyme that acts in 5-KETE biosynthesis, which is a highly novel and interesting<br /> mechanism. Under stress conditions, DHRS7 facilitates rapid inflammatory<br /> signaling and leukocyte recruitment through the 5-KETE pathway.<br /> Major Comments<br /> Identification of DHRS7 as a 5-HEDH Candidate<br /> The screening successfully identified DHRS7 as a candidate enzyme with 5-<br /> HEDH activity. LC-MS profiling of wild-type cell lines revealed increased 5-KETE<br /> levels in cells exposed to 5-HEDE and vice versa, with a stronger effect observed<br /> in 5-KETE accumulation. Surprisingly, 5-KETE production appeared to be<br /> favored under non-stress conditions. We would like to see a description of the<br /> data normalization to exclude the possibility that these differences arise from<br /> variations in cell viability, abundance, or any other experimental conditions.<br /> Alternative Pathways and Metabolic Compensation<br /> Another observation is the reduction in 5-KETE and 5-HETE levels in DHRS7<br /> knockout cells, corroborating the proposed DHRS7 role. But the persistence of<br /> these metabolites in silenced cells even at lower concentrations is curious, which<br /> leads to a few hypotheses such as the activation of endogenous compensatory<br /> mechanisms and exogenous uptake of these metabolites from the media. To<br /> further investigate the origin of these residual metabolite levels, it is essential to<br /> quantify 5-KETE and 5-HETE in the culture medium to test if the cells' knockouts<br /> exposure to these lipids could explain these residual levels. To evaluate if these<br /> residual metabolites could have originated from endogenous mechanisms, a<br /> transcriptome analysis could be used to identify other redox-active enzymes<br /> differentially expressed that could exhibit potential 5-HEDH activity thereby<br /> compensating DHRS7 silencing.<br /> Subcellular Localization of DHRS7<br /> The authors employed GFP-tagged DHRS7 constructs for subcellular localization<br /> and genetic complementation assays in DHRS7 KO A549 cells and zebrafish<br /> Dhrs7 KO models. This strategy successfully restored the wild-type phenotype,<br /> as evidenced by increased 5-HETE and 5-KETE levels upon treatment with<br /> precursors, corroborating the initial hypothesis of DRS7 as a 5-HEDH. However,<br /> the conclusion that DHRS7 localizes to microsomes lacks experimental<br /> validation, as no microsomal markers were used in confocal imaging. Indeed,<br /> cellular fractionation and Western blot assays indicate DHRS7 also localized in<br /> the nucleus, granules, and microsomes, but GFP fluorescence was absent in the<br /> nucleus. Given that the antibody used for Western blotting was available, it’s not<br /> clear why the authors did not employ an anti-DHRS7 antibody for<br /> immunofluorescence to precisely determine its intracellular distribution rather<br /> than relying on GFP-based localization assays.<br /> Kinetic Characterization of DHRS7 Activity<br /> The authors conducted enzymatic kinetics assays for DHRS7 and applied a<br /> Michaelis-Menten model for data fitting. However, the fitting shows clear<br /> deviations, with a notably low coefficient of determination (R²), suggesting that<br /> this model may not adequately describe DHRS7’s catalytic properties. In fact, a<br /> typical Michaelian model does not appear to fit the data distribution. To ensure<br /> that these discrepancies are not due to experimental artifacts, we recommend<br /> repeat the experiments performing additional replicates. Furthermore,<br /> considering the probable reversibility of 5-KETE conversion, alternative kinetic<br /> models that account for this factor should be explored.<br /> Minor Comments<br /> ● Lines 13-15: The authors state, "As the DHRS7 (but not DHRS3)<br /> knockdown effect was consistent with 5-HEDH activity, we tested whether<br /> DHRS7 also promoted 5-KETE reduction. This was the case." However,<br /> Figure S1D shows a reduction in 5-HETE, not 5-KETE. More clarification<br /> is needed.<br /> ● Cell Line Justification: The authors discuss DHRS7 expression in<br /> various contexts but do not justify their choice of A549 cells. Since none<br /> of the cited references mention DHRS7 expression in this line, a<br /> description of the rationale for model choice is necessary.<br /> ● Figure 1E: We recommend a dose-time response curve for DOX<br /> treatment to monitor DHRS7 expression levels. This would determine if<br /> DHRS7 expression remains at physiological levels or becomes<br /> supraphysiological, thereby ensuring that subsequent treatments also<br /> occur under physiological conditions.<br /> ● Figure 1F: We recommend a more clear description that these are cells<br /> lacking the DHRS7 construct to enhance reader understanding.<br /> ● Figure 2B: H₂O₂ is not a direct intermediate in the 5-HETE/5-KETE<br /> pathway, though it may indirectly influence it by activating 5-LOX, altering<br /> redox balance (NADP⁺/NADPH), and contributing to ferroptosis. The<br /> statement "Lipid peroxidation stimulates 5-KETE production through<br /> DHRS7" would be more robust if 5-LOX activity was assessed. We<br /> suggest a validation experiment: Treat DOX-induced DHRS7-expressing<br /> cells with H₂O₂ and measure markers of lipid peroxidation, such as<br /> malondialdehyde (MDA), isoprostanes, or 4-hydroxy-2-nonenal (4-HNE).<br /> This would confirm lipid peroxidation’s role in 5-KETE production.<br /> ● Figure 3D: Overexpression methodology in HEK cells is unclear. The<br /> knockout was achieved using CRISPR/Cas9, not shRNA. More<br /> clarification is needed on whether overexpression was introduced via a<br /> separate construct post-knockout, whether a CRISPR activation<br /> (CRISPRa) or DOX-inducible system was used, or if overexpression was<br /> performed in a different cell line.<br /> ● Figure 4A: The heatmap visualization of metabolite concentrations was<br /> clear, but cluster analysis would provide more information related to the<br /> significance of observed alterations.
On 2025-03-22 16:55:34, user Kelsey Gray wrote:
This work has been published by the journal, Fungal Biology and Biotechnology - https://fungalbiolbiotech.biomedcentral.com/articles/10.1186/s40694-024-00191-4/metrics
On 2025-03-21 21:18:05, user Jeffrey J. Gray wrote:
Can you please add the link to the published article? (title has changed)<br /> https://www.sciencedirect.com/science/article/pii/S2405471225000341
On 2025-03-21 20:46:21, user Bailey Bowcutt wrote:
I believe this paper has been published with Antimicrobial Agents and Chemotherapy. The DOI: https://doi.org/10.1128/aac.00207-19
On 2025-03-21 15:31:16, user Peter Diebold wrote:
Great work here! Looking through the metadata, I have a small suggestion. Could you include the full GTDB taxonomy in future versions?
Secondly, I'd suggest renaming the "dustbin" to something that doesn't imply trash. Seems like a large amount of the bacterial diversity is in the dustbin and the name could lead someone to incorrectly assume that they aren't important as was done in this paper https://doi.org/10.1093/bioinformatics/btae717 <br /> Lastly, I'd really love to see a few more basic statistics about what is in the database. Perhaps recreate some of the tables and figures that GTDB makes https://gtdb.ecogenomic.org/stats/r220 <br /> Thanks again for the great work!
EDIT:
I realized that you did not use GTDBtk to assign taxonomy but used Sylph. Then I guess you parsed the species name from the contigs? Unfortunately this will not provide the accurate taxonomy because GTDB does not correct the taxonomic names in each of the assemblies in the database. Very often the contig names and taxonomies do not match the taxonomy assigned by GTDB. This is a critical error in my opinion, but could be solved by simply building a table to associate the correct taxonomy for each contig. A better solution would be to run GTDB-tk on all the assemblies, but I understand this would take considerable time.
On 2025-03-21 13:57:33, user Rubayet Elahi wrote:
Now published in EMBO Reports https://www.embopress.org/doi/full/10.1038/s44319-025-00420-w
On 2025-03-20 14:53:04, user Ana wrote:
This preprint has been published. You can see it in the following link: https://doi.org/10.1186/s10194-025-01969-6
On 2025-03-19 20:10:32, user Lorenzo Calviello wrote:
Amazing work! Any chance to have the mapped crosslinks available (e.g. as bigwig files)?
On 2025-03-19 18:15:47, user Ana Nascimento wrote:
The peer-reviewed version of this pre-print can be found at: https://www.nature.com/articles/s41598-020-69944-6
On 2025-03-18 20:10:33, user Marie Moinet wrote:
I think the title should read P681H, not P680H
On 2025-03-18 19:59:26, user Brett Pike wrote:
Hello, thank you for sharing this mountain of data. In my preliminary evaluation I find that the orientation of the chromosomes is not standardized, i.e. about half need to be reverse complemented. I am writing to ask that you fix this, and I suggest using the orientation from cs10. ntSynt-viz with '--normalize' flag I find to be the simplest visualizer for this task. Thank you!
On 2025-03-18 13:47:33, user Andreas Bueckle, Ph.D. wrote:
Please note that this paper was published in Nature Methods on Thu, Mar 13, 2025: https://www.nature.com/articles/s41592-024-02563-5
On 2025-03-17 18:50:48, user Catherine Douds wrote:
Thank you so much for sharing this work, it’s a really great paper. My biggest criticism is that the methods section does not clearly define how the Ribo-seq and RNA-seq were aligned. Did you align with a different transcript or for each dataset? Or was there one transcript all data were aligned to? I’d love to see a more detailed methods section in the final version.
On 2025-03-17 14:47:54, user Simak Ali wrote:
Now published in Cancer Research. DOI: 10.1158/0008-5472.CAN-24-0013
On 2025-03-17 07:38:26, user YQ Hu wrote:
This preprint has been published in Nature entitled "Plasma proteomic associations with genetics and health in the UK Biobank (doi: 10.1038/s41586-023-06592-6)“ in 2023.
On 2025-03-16 17:51:31, user Paul Macklin wrote:
This is now published here:
On 2025-03-15 05:20:17, user Stef wrote:
Interesting approach. It would be interesting to compare with sccomp. A count-based sum-contrained Beta-Binomial model https://doi.org/10.1073/pnas.2203828120
On 2025-03-15 04:05:42, user Min Zhu wrote:
The full version of this manuscript is online in Science Advances. https://www.science.org/doi/10.1126/sciadv.adt7274
On 2025-03-15 03:29:36, user Spencer Williams wrote:
The title is misleading. This paper is not about chaotropic agents. Remove this tangential information from title and abstract
On 2025-03-14 21:15:12, user Rajendra K C wrote:
We discussed this paper in our RNA journal club. We found the discovery of this novel splicing mechanism quite interesting, which seems like a last-resort strategy for cells to remove transposons that have already integrated into exons while still retaining some level of functional protein. The mutagenesis experiment to identify SOS splicing factors was particularly interesting. One question that came up in our discussion: What happens to the excised transposon post-SOS splicing? Is there any evidence that it gets degraded or reintegrated elsewhere in the genome?
On 2025-03-14 16:26:21, user staszek sdh wrote:
On 2025-03-14 11:51:35, user Jacob Hanimann wrote:
Love the approach of mixing morphology with molecular state in patient tissue for the identification of new biomarkers!
On 2025-03-14 06:51:45, user Thomas Bradley wrote:
This looks like great work, but I feel our prior work on this topic should have been cited ( https://www.nature.com/articles/s41467-023-39867-7 ) especially as we arrive at similar conclusions
On 2025-03-14 04:31:15, user makotokun wrote:
Introductin: "Though such mutations are rare, mammalian embryos and placentae face unique challenges during normal development that can impose GIN 1."<br /> 1. Why mammal is unique for the challenges of GIN? I can not find answer from Ref.1.<br /> 2. I believe the "placentae" should be "placenta".
On 2025-03-13 23:38:50, user Jesus Montoya wrote:
This seems to have been published last year in Communications Biology: https://www.nature.com/articles/s42003-024-07147-9
On 2025-03-13 13:24:44, user Justina Zvirblyte wrote:
Published: https://www.nature.com/articles/s42003-024-06478-x
On 2025-03-13 13:09:46, user marodon wrote:
Related to "Somewhat paradoxically, a recent pre-print study demonstrated a small but statistically significant decrease in basal heat sensitivity in both female and male mice conditionally depleted for Penk expression in systemic Tregs. Mechanical thresholds and other sensory modalities were however not examined ". This sentence is not accurate since the preprint had been significantly improved and was published in eLife as a Version of Record (VOR) in August 2024. Various mechanical tests were performed and are shown in a supplementary figure in the VOR. Moreover, mice depleted of Penk in Treg do not show a decrease in basal heat sensitivity but an increase (they are more sensitive @55° than the controls). These results are confirmed by Mendoza et al using the same mouse model. Best regards
On 2025-03-13 10:31:41, user Diethard Tautz wrote:
There are two key conclusions in this paper: 1) an ancestral origin of house mice from the Indo-Pakistan region and 2) incomplete lineage sorting for the observed alle sharing between contemporary populations.
Both conclusions are not sufficiently supported, given the current published evidence. I suggest that the authors carefully study this previous evidence and adjust their conclusions accordingly.
Origin of the house mouse radiation<br /> To trace the region of origin based on population genetic data, requires sufficient sampling of the relevant regions and comparable sample structures. The broadest samplings available to date that address the question of the origin are published in (Afzali, 2024; Hardouin et al., 2015). They show a high diversity of lineages in Iran and a complex history of populations across Asia. <br /> Lawal and Dumont include only one population from Iran, but do not capture the full diversity that is already known from there.<br /> Further, some of the population samples used by Lawal and Dumont represent sampling from local regions, while others are from broad regions (PAK and IND). Given the known deme structure in mice (Linnenbrink, Teschke, Montero, Vallier, & Tautz, 2018), the broad samplings of PAK and IND may cover different lineages that should not be lumped into a single one. This issue would need a deeper attention in the overall analysis.
Incomplete lineage sorting instead of introgression<br /> This issue has been addressed in a large number of papers. All of these authors have carefully evaluated the two alternatives. The analysis presented by Lawal and Dumont is too superficial to make a strong claim that runs contrary to all of these previous data and analysis. <br /> Probably the strongest argument against incomplete lineage sorting is the existence of large introgressed haplotypes that segregate in the different subspecies and species and that were found to be subject to adaptive introgression (Song et al., 2011; Staubach et al., 2012). Several of such regions have subsequently been studied in detail and the long haplotype structures were confirmed, e.g. in (Banker, Bonhomme, & Nachman, 2022; Hasenkamp, Solomon, & Tautz, 2015; Linnenbrink, Ullrich, McConnell, & Tautz, 2020). <br /> Neither incomplete lineage sorting, nor long-term balancing selection can explain the existence of such long introgressed haplotypes, since they would be broken up by recombination over time. Note that although the mouse lineage divergence times seem "shallow" with being shorter than 0.5 Million years, the number of generations is actually high, given the short generation times. To suggest that incomplete lineage sorting is a possible explanation for the shared alleles would require to show with appropriate simulations that long haplotypes could be retained over hundreds of thousands of generations without breaking them up.<br /> Such simulations have been extensively used for the comparisons between Neandertals and humans, where introgression at specific loci is distinguished from ILS by comparing expected haplotype lengths.
Afzali, Y. (2024). Asian Mus musculus: subspecies divergence, genetic diversity, and historical biogeography. JOURNAL OF MAMMALOGY, 105(6), 1378-1391. doi:10.1093/jmammal/gyae075<br /> Banker, S., Bonhomme, F., & Nachman, M. (2022). Bidirectional Introgression between Mus musculus domesticus and Mus spretus. GENOME BIOLOGY AND EVOLUTION, 14(1). doi:10.1093/gbe/evab288<br /> Hardouin, E. A., Orth, A., Teschke, M., Darvish, J., Tautz, D., & Bonhomme, F. (2015). Eurasian house mouse (Mus musculus L.) differentiation at microsatellite loci identifies the Iranian plateau as a phylogeographic hotspot. Bmc Evolutionary Biology, 15. doi:10.1186/s12862-015-0306-4<br /> Hasenkamp, N., Solomon, T., & Tautz, D. (2015). Selective sweeps versus introgression - population genetic dynamics of the murine leukemia virus receptor Xpr1 in wild populations of the house mouse (Mus musculus). Bmc Evolutionary Biology, 15. doi:10.1186/s12862-015-0528-5<br /> Linnenbrink, M., Teschke, M., Montero, I., Vallier, M., & Tautz, D. (2018). Meta-populational demes constitute a reservoir for large MHC allele diversity in wild house mice (Mus musculus). Frontiers in Zoology, 15. doi:10.1186/s12983-018-0266-9<br /> Linnenbrink, M., Ullrich, K. K., McConnell, E., & Tautz, D. (2020). The amylase gene cluster in house mice (Mus musculus) was subject to repeated introgression including the rescue of a pseudogene. Bmc Evolutionary Biology, 20(1). doi:10.1186/s12862-020-01624-5<br /> Song, Y., Endepols, S., Klemann, N., Richter, D., Matuschka, F. R., Shih, C. H., . . . Kohn, M. H. (2011). Adaptive Introgression of Anticoagulant Rodent Poison Resistance by Hybridization between Old World Mice. Current Biology, 21(15), 1296-1301. doi:10.1016/j.cub.2011.06.043<br /> Staubach, F., Lorenc, A., Messer, P. W., Tang, K., Petrov, D. A., & Tautz, D. (2012). Genome Patterns of Selection and Introgression of Haplotypes in Natural Populations of the House Mouse (Mus musculus). Plos Genetics, 8(8). doi:10.1371/journal.pgen.1002891
On 2025-03-12 17:30:11, user xyz wrote:
I read your paper the study is nice but I have certain questions regarding your paper<br /> 1. In figure 5 why the percentage of macrophage with phagocytosis and trogocytosis in case of suspended cells same.<br /> 2. In figure 6 can you please confirm what was the effect on macrophage trogocytosis on increasing the cell adhesion<br /> 3. Also what was the cell nature adherent or suspended when you din different integrin knockout<br /> Hope to hear from you back
On 2025-03-12 09:54:00, user achilleas_frangakis wrote:
It appears that the molecular architecture of the kidney slit diaphragm is evolutionarily conserved from Drosophila to mice!
On 2025-03-12 03:33:39, user Researcher_872 wrote:
RNA sequencing and proteomics data indicate that midnolin is expressed ubiquitously across a wide range of cell lines and tissues (DepMap and Proteinatlas). Therefore, it is unclear why the authors suggest in the abstract that midnolin is predominantly expressed in lymphocytes.
A previous BioRxiv paper reports the structure of midnolin bound to the proteasome (PMID: 40027645), which was not acknowledged or cited in this paper. The authors cannot state the mechanism is "unknown" when there is a 2023 Science paper describing the mechanism (PMID: 37616343). Furthermore, there is a 2016 Dev Cell paper (PMID: 27326929) that is the first to explore the role of midnolin in vivo and its interaction with the proteasome, which was also not cited in this preprint or the authors' previous paper (PMID: 38625151).
Overall, the authors should be more mindful of the literature and accurately cite seminal papers that preceded their work.
On 2025-03-11 16:46:46, user Nikhil Thomas wrote:
This manuscript has been published in PLoS Genetics at the following link:<br /> https://doi.org/10.1371/journal.pgen.1011370
On 2025-03-11 05:53:34, user John Golz wrote:
This manuscript has now been published and a link to the publication could now be included.
https://doi.org/10.1186/s12896-024-00864-3
Thanks
On 2025-03-10 19:52:40, user Sr. Galán wrote:
A peer reviewed version of this article is now published in Ecosistemas, link here:<br /> https://www.revistaecosistemas.net/index.php/ecosistemas/article/view/2847
On 2025-03-10 04:21:18, user Young Cho wrote:
Dear Authors,<br /> Thank you for sharing your insightful work, "In Silico Engineering of Stable siRNA Lipid Nanoparticles: Exploring the Impact of Ionizable Lipid Concentrations for Enhanced Formulation Stability." Your study makes an important contribution to the field of lipid nanoparticle (LNP) research by highlighting the role of ionizable lipid concentrations in siRNA encapsulation and stability. The use of coarse-grained molecular dynamics (MD) simulations and steered molecular dynamics (SMD) provides a detailed molecular-level understanding of LNP formation, which is particularly valuable for optimizing RNA-based drug delivery systems.<br /> Summary<br /> This study examines how neutral and positive ionizable lipids influence LNP stability and siRNA encapsulation efficiency. The findings indicate that LNPs with positive ionizable lipids encapsulate siRNA more effectively than those with neutral lipids, likely due to their integration with phospholipids and the prevention of siRNA escape. Interestingly, low and medium concentrations of both neutral and positive DLKC2 showed better compartment formation and encapsulation efficiency compared to high concentrations. Additionally, neutral lipids exhibited greater aggregation, which could impact LNP stability.<br /> Introduction<br /> Your introduction effectively establishes the relevance of this study by situating it within the broader context of LNP research. The discussion of existing challenges in siRNA delivery and the role of lipid composition is well-articulated. However, further elaboration on how your study builds upon previous experimental findings could help connect computational insights with practical applications.<br /> Results<br /> The figures and data presentation generally support your conclusions. Figure 4, which illustrates LNP compartment formation at different lipid concentrations, is particularly valuable in showing how high concentrations lead to instability. We do think that some quantitative metrics such as bilayer thickness, lipid density, or compartment size would enhance the strength of these findings. Additionally, since water is omitted from the visualizations for clarity, we think it would be beneficial to include a figure that shows water so we can visualize the hydration effects and lipid-water interactions.<br /> Discussion<br /> Your discussion effectively compares findings with prior studies, reinforcing that positive ionizable lipids enhance siRNA encapsulation and that lipid aggregation in neutral systems may reduce stability. While you mention previous molecular dynamics studies (e.g., Paloncýová et al. and Trollmann & Böckmann), we feel a more direct comparison of numerical data and trends from these works would further contextualize your results. Additionally, discussing potential experimental validation techniques (e.g., cryogenic electron microscopy or encapsulation efficiency assays) could provide future directions for integrating simulations with laboratory-based studies. However, that is just our opinion as we do understand that this study takes on a more computational approach and is still very impactful.<br /> Suggestions for Improvement<br /> 1. Expand quantitative analysis in Figure 4 by including measurements of bilayer thickness, lipid density, and compartment size to provide a more rigorous validation of LNP stability.<br /> 2. Clarify the role of hydration in lipid-water interactions since water was omitted in visualizations.<br /> 3. Strengthen comparisons with previous molecular dynamics and experimental studies by integrating direct numerical contrasts.<br /> 4. Discuss potential experimental validation approaches that could complement your computational findings and enhance their real-world applicability.<br /> Final Thoughts<br /> Overall, this paper presents a well-structured and valuable contribution to siRNA delivery research. With minor refinements in quantitative analysis, literature comparisons, and discussion of experimental validation, the study could be even more impactful. Thank you for your efforts in advancing the field of LNP-based RNA therapeutics!<br /> Best regards,<br /> UHM MBBE 602 Graduate Students
On 2025-03-10 04:17:10, user Young Cho wrote:
Summary:<br /> This study provides a comprehensive analysis of miRNA profiles in Culex tarsalis, identifying 86 known miRNAs and 20 novel miRNAs, is a significant contribution to the field of insect molecular biology and vector research. This works sets the foundation for future studies on gene regulation and host-pathogen interactions in Cx. tarsalis, a major vector of West Nile Virus (WNV). While the methodology is robust and the findings are compelling, the paper would benefit from some minor revisions to strengthen data presentation, clarify experimental choices, and align its conclusions more closely with the results. <br /> Introduction: <br /> The introduction frames the importance of miRNA research in Cx. tarsalis well, particularly in the context of understanding its role as a vector for WNV. However, the title of the paper may be misleading since the findings do not directly link the identified miRNAs to WNV vectoring. Reframing the title and introduction to focus on the broader importance of miRNA characterization in Cx. tarsal without overemphasizing the WNV connection would improve clarity and prevent misalignment between the study’s scope and its claims. <br /> Results: <br /> The results section presents a comprehensive dataset of miRNAs identified through computational comparison with other mosquito species and validated using RT-qPCR. The discovery of novel miRNAs and the observed isomiR variations are particularly noteworthy, with the predominance of 3’ end insertions being a finding of potential significance in gene regulation. That said, clearer justification for the selection of the 10 miRNAs validated by qPCR would strengthen the interpretability of the results. <br /> Discussion: <br /> The discussion effectively places the study’s findings within the broader context of existing research on mosquito miRNAs and draws meaningful comparisons with other species like Aedes albopictus and Cx. quinquefasciatus. The evolutionary conservation of miR-184 and the identification of unique miRNAs in Cx. tarsalis offer valuable insights. However, the paper would benefit from further discussion on the functional implications of these miRNAs, particularly their potential roles in development, immunity, and host-pathogen interactions. Additionally, the observed differences in miRNA expression between cell lines and whole organisms raise important questions that warrant more exploration. <br /> Suggestions: <br /> 1. Revise the title to better reflect the study’s current findings and avoid overemphasizing WNV. <br /> 2. Clarify the rationale behind the selection of the 10 miRNAs for qPCR validation. <br /> 3. Expand the discussion on the functional roles of the identified miRNAs and their potential involvement in host-pathogen interactions. <br /> 4. Address the limitations more explicitly, such as the reliance on a single genome assembly, the lack of data from different mosquito life stages and tissues, and the absence of additional validation methods like Northern blot. <br /> 5. Consider including a statistical analysis to highlight differences in miRNA expression between cell lines and whole organisms. <br /> 6. Discuss the potential influence of feeding behavior on gene expression and its relevance to vector competence.
On 2025-03-09 11:44:16, user Jake Ivan P. Baquiran wrote:
Now published in Environmental Microbiology doi: 10.1111/1462-2920.70041
On 2025-03-07 18:39:57, user Randall Eck wrote:
Exciting article! Given the role of 3' UTR alternative polyadenylation (APA) in RNA localization and stability (PMC9261900) and the role of TDP-43 in regulating 3' UTR APA (PMC10849503), is there a relationship between TDP-43 regulation of RNA localization and 3' UTR APA in your data?
On 2025-03-07 12:28:58, user Marc RobinsonRechavi wrote:
Under Data Accessibility, the authors write:
Data and R code sufficient to replicate all analyses will be made publicly available upon acceptance of this manuscript for publication.
This is a publication, i.e. it is made public as part of the scientific record and is citable, thus I strongly invite the authors to make the corresponding data and code available without delay.
On 2025-03-07 07:27:12, user Marc RobinsonRechavi wrote:
Under Code Sharing Plan, the authors write:
All the code used for the generation of datasets and subsequent analysis will be made publicly available in<br /> a GitHub repository upon publication
This is a publication, i.e. it is made public as part of the scientific record and is citable, thus I strongly invite the authors to make the corresponding code available without delay.
On 2025-03-06 09:47:18, user Alexei Korennykh wrote:
As a corresponding author, Alexei Korennykh hereby documents the timeline of our discovery of Nocturnin NADP(H) phosphatase activity.
[2018, December 17]<br /> Our Manuscript "The Metabolites NADP+ and NADPH are the Targets of Circadian Protein Nocturnin (Curled)" was submitted to a high-quality journal (per BioRxiv policy journal name cannot be mentioned here) (under id ....2018-12-17736A)
[2018, December 19]<br /> The editor sends the work to referees.
[2018, December 21]<br /> We submit our Nocturnin-NADP co-crystal structure to the PDB database and obtain PDB ID 6NF0.
https://www.rcsb.org/structure/6NF0 has the following permanent record:
Deposited: 2018-12-18 <br /> Released: 2019-05-01 <br /> Deposition Author(s): Estrella, M.A., Du, J., Korennykh, A.
[2019, January 15]<br /> Journal rejects the manuscript, based substantially on negative remarks of Ref#3, who is “an expert on Nocturnin”:
Referee expertise:
Although we responded that all concerns can be addressed directly and without experiments, the journal is not willing to re-consider our work.
[2019, January 30]<br /> We posted our manuscript here, to BioRxiv and it became available to the public.
[2019, March 28] <br /> We submitted the paper to the final publishing journal (see top of the page, "Now published in ") and the paper was received and sent for review.
[2019, April 18] <br /> The paper was accepted (see top of the page, "Now published in ").
[2019, May 30] <br /> The paper was published (see top of the page, "Now published in ").
[2019, June 5] <br /> Alexei Korennykh wrote to change Uniprot annotation of Nocturnin
Wed Jun 05 05:20:37 2019, akorenny@princeton.edu wrote:
Major changes in NOCT (CCRN4L) gene function and description. <br /> Source:<br /> https://www.nature.com/articles/s41467-019-10125-z <br /> Suggested revisions:
"Circadian deadenylase"<br /> changes to<br /> "Circadian NADP(H) phosphatase"
"Catalytic activity: Exonucleolytic cleavage of poly(A) to 5'-AMP. EC:3.1.13.4"<br /> changes to:<br /> "Catalytic activity: 2'-Phosphate removal from NADP+ and NADPH. EC:to be created"
[2019, June 7] <br /> UniProt Begins re-annotation<br /> Dear Alexei,
Thank you for having submitted a request for the update of a UniProtKB entry.
Your request has already been sent to an annotator and will be handled with<br /> high priority.
We will send you an e-mail when the update is completed.
Best regards
SP
[2019, July 1] <br /> UniProt changes Deadenylase to Phosphatase for Nocturnin:
Dear Alexei,
Thank you for passing on the details of your recent paper. The nocturnin <br /> entry has been updated and will be available as part of UniProt release <br /> 2019_08 on 18th September. In the meantime, I have included the entry <br /> below in text format. Please feel free to get back in touch if you have <br /> any comments about the content.
Kind regards,<br /> MM
ID NOCT_HUMAN Reviewed; 431 AA.<br /> AC Q9UK39; D3DNY5; Q14D51; Q9HD93; Q9HD94; Q9HD95;<br /> DT 02-NOV-2001, integrated into UniProtKB/Swiss-Prot.<br /> DT 04-NOV-2008, sequence version 2.<br /> DT 31-JUL-2019, entry version 148.<br /> ……<br /> CC NAD(+) and of NADPH to NADH (PubMed:31147539). Shows a small<br /> CC preference for NADPH over NADP(+) (PubMed:31147539). Represses<br /> CC translation and promotes degradation of target mRNA molecules<br /> CC (PubMed:29860338
…
[2019, July 1]
Up to this date (i.e. 5 months since our BioArxive paper became publically available) no work by others, which described Nocturnin as NADP(H) phosphatase was published or submitted to any journal, to the best of our knowledge.
On 2025-03-06 02:33:06, user Charles Warden wrote:
Thank you very much for posting this preprint!
The "Code availability" section indicates "We provide supplementary files containing an R script with functions to run our CRF-based correction procedure as well as a tutorial notebook illustrating how to run it.".
However, I think I see anything uploaded as supplemental files. Am I overlooking anything, or does the supplemental code need to be added in a revision?
Thank you very much!
Sincerely,<br /> Charles
On 2025-03-06 00:00:06, user Laura Lackner wrote:
An updated version of this preprint has been published in MBoC - https://doi.org/10.1091/mbc.E23-05-0168 . The revised and accepted version has a slight modification to the title.
On 2025-03-04 21:05:38, user Simone Picelli wrote:
Hi, I think there is a mistake in the name of the company used to make the modified TSO. It's not Biosyn Corporation ( http://biosyncorp.com ), as you wrote, but rather Bio-Synthesis ( http://biosyn.com ). <br /> Moreover, in the TSO sequence: "/5Biosg/" is the acronym used by IDT for a 5' biotin. The "g" has nothing to do with deoxyguanosine (G), but you write in the paper "5BiosG/" and this can be confusing. The standard 10x TSO sequence is, in fact: 5’-AAGCAGTGGTATCAACGCAGAGTACATrGrGrG-3’<br /> so no G at the 5' (like there was never a G at the 5' of the SMART-seq oligo, from which 10x took their sequence).<br /> The code for biotin at Biosyn is [Btn] (standard C6 spacer, which I assume is the one you mean here).
On 2025-03-04 02:45:42, user Andrei Drabovich wrote:
Interesting technology, but Table 2 "Total Ion Usage Rate" calculations for timsTOF vs SLIM-QTOF are not clear.<br /> Seems like all major advantages in numbers are due to "TOF transmission efficiency" but not to ion mobility.
On 2025-03-04 02:21:17, user Nelly Olova wrote:
This work has now been published in the Methods in Molecular Biology book series, volume 2866 (Springer Nature)
On 2025-03-03 17:25:34, user Johannes Daniel Scharwies wrote:
This is the author's version of the work. It is posted here by AAAS for personal use, not for redistribution. The definitive version was published in Science on 6 Feb 2025, DOI: 10.1126/science.ads5999.
On 2025-03-03 16:11:50, user hansdb wrote:
One Corded Ware (CGG107476) and two Bell Beaker individuals (CGG106805 and CGG106737) from your interesting study belong to Y-DNA haplogroup I2-L38 (aka I2a1b2a).<br /> As decribed in my citizen scientist paper ( https://www.academia.edu/115363574/RECONSTRUCTING_THE_JOURNEY_OF_Y_DNA_HAPLOGROUP_I2_S2555_TO_I2_L38_Tracing_Genetic_Footprints_Across_Time_and_Space ) this haplogroup was also related to:<br /> * an EBA Unetice sample from Germany (I0114)<br /> * an EBA Unetice sample from Bohemia (I7959)<br /> * an IA Hallstatt sample from Germany (MBG008)<br /> * an IA La Tène sample from Bohemia (I17327)<br /> * an IA La Tène sample from France: GLN32
Most interestly this haplogroup also occured among the Urnfield epoch Lichtenstein clan from Osterode-am-Harz. Since it is mentioned (paragrapghs 194 to 196) that very few genomes from the Urnfield Culture exist (as a result of the cremation practice) it would be interesting if the well-preserved samples of the Lichtenstein cave could be integrated in your study.
On 2025-03-03 14:46:23, user Elisa Rosati wrote:
A couple of questions:<br /> 1) How can you be sure that the MAIT cells you observed are not bystander activated during the T cell stimulation and thus not really Myelin-specific? I would perhaps perform the experiments with two additional setups:<br /> a) MHC-blockage (If MAIT cells are really specific they should appear here) <br /> b) MR1-blockage (if MAIT cells are specific and activated via TCR they should not appear here)
2) Have you tried to perform the analyses separately for HLA-DRB1*15:01 positive and negative individuals separately? It was shown by a study from Adaptive Biotechnology that a limited number of TCR clusters enriched in MS exist and that these clusters are mostly CD4 and very different in DRB1*15:01 positive and negative individuals.
On 2025-03-03 06:36:55, user Siddhartha Saha wrote:
Very insightful article. there was another outbreak of avian influenza among tigers in a nearby area around same time, so wondering whether any relation to that outbreak has been ruled out. Even in that outbreak, specimens were sent to NIHSAD ( https://www.thehindu.com/sci-tech/energy-and-environment/leopard-three-tigers-die-of-avian-flu-in-maharashtras-gorewada-rescue-centre/article69064307.ece )
On 2025-03-02 15:54:05, user Ambrose, Zandrea wrote:
This study has been peer reviewed and published: https://journals.asm.org/doi/10.1128/mbio.00169-25
On 2025-03-01 00:59:54, user Tim wrote:
While groundbreaking, I wish this paper expanded up author N.R.B.’s de novo inclusion of huel in the fine tuning of the RFDiffusion network compared to the characterization of fermented yeast to acetaldehyde formation chain on massive (1 million samples or more) scales.
On 2025-02-28 12:53:50, user Prof. T. K. Wood wrote:
l 339: Paris is a toxin/antitoxin system and TAs are the most-prevalent phage inhibition system; this should be noted.
l 365: The seminal identification of of TAs and phage inhibition (1996) should cited:<br /> doi: 10.1128/jb.178.7.2044-2050.1996
On 2025-02-28 10:05:42, user Giampaolo Minetti wrote:
This preprint has now been published as a peer reviewed, open access article in Cell Death Discovery:<br /> Minetti G, Dorn I, Köfeler H, Perotti C, Kaestner L. Insights from lipidomics into the terminal maturation of circulating human reticulocytes. Cell Death Discov. 11, 79 (2025). doi: /10.1038/s41420-025-02318-x<br /> Stable, shortened URL:<br /> https://rdcu.be/ebvgH
On 2025-02-28 08:34:44, user Bjarke Jensen wrote:
Dear authors,
Congratulations with this interesting study.
In my view it would be helpful if you further develop the descriptions of the state of trabeculation. For example, did you make measurements (counting, thicknesses, proportions) of the trabecular and compact layer, what were the values and how do they relate to diagnostic criteria associated with trabeculation? It would also be helpful if you support this part of your Results with clinical imaging (echocardiography and CMR) onto which is shown the measurements (or overt phenotype) that led to the interpretation of 'hypertrabeculation'. I for one would not mind a full text figure dedicated to this part. <br /> Part of the reason for giving these suggestions is of course that your title states 'hypertrabeculation' while the associated phenotyping is proportionally very small and accordingly a bit unclear.
Best wishes and good luck with the publication.
Bjarke
On 2025-02-27 23:06:56, user Yuliana Pullas wrote:
Hi,<br /> 1. In your text you have "Consistent with proteins accounting for 13–23% of EPS (Fig. 3A)" I think it is Fig. 2A.
On 2025-02-27 20:34:24, user Michael Roswell wrote:
This paper was published in January, 2025 https://onlinelibrary.wiley.com/doi/10.1111/ddi.13969
On 2025-02-27 17:50:50, user Maxwell Neal wrote:
A peer-reviewed version of this article has been published by Nucleic Acids Research: Genomics and Bioinformatics<br /> https://doi.org/10.1093/nargab/lqaf008
On 2025-02-27 16:02:16, user Pär Jonsson wrote:
Article: https://doi.org/10.1021/acs.jcim.4c01799 <br /> Code & Data: https://github.com/edvinforsgren/OPLS-HDA
On 2025-02-27 04:18:23, user Manoj Menon wrote:
Published now in Molecular & Cellular Biology https://doi.org/10.1080/10985549.2025.2454421
On 2025-02-27 02:16:06, user Le Zhen wrote:
Now this manuscript has been accepted for publication in the journal Biomaterials, with a new title: Synthetic Vascular Graft That Heals and Regenerates (doi: https://doi.org/10.1016/j.biomaterials.2025.123206) .
On 2025-02-26 17:21:48, user Leonardo Di Bari wrote:
Thanks for the analysis, the study is promising. I am, Leonardo Di Bari, a PhD student in the SPQB ( https://sites.google.com/view/spqb ) group of Martin Weigt and Francesco Zamponi: we have utilized the entropy that you present in the following three articles.<br /> https://arxiv.org/pdf/2412.01969 <br /> https://www.pnas.org/doi/abs/10.1073/pnas.2406807121 <br /> https://www.nature.com/articles/s41467-022-31643-3 <br /> I think it would be interesting to maybe compare the two formulations. <br /> Best regards,<br /> Leonardo Di Bari
On 2025-02-26 10:03:48, user Young Cho wrote:
This is a comment from a Journal Club of MBBE 602 in Univ of Hawaii.
Summary<br /> This paper explores the capabilities of twin prime editing (twinPE) for large DNA sequence modifications, including deletions, replacements, integrations, and inversions. The authors demonstrate the efficiency of twinPE in human cells (HEK293T & Huh7) and its potential for therapeutic applications when combined with the Bxb1 integrase. Key findings include precise and flexible editing with fewer indels, high knock-in efficiency, and the ability to bypass certain DNA repair pathways. However, the study lacks long-term data on genomic stability and scalability for human applications, and some experimental details and comparisons with other gene-editing techniques are insufficiently explored.
Introduction<br /> The introduction provides a solid foundation for the study but could benefit from more background information on the therapeutic applications explored, as well as the mechanism that resulted in limitations relating to the pegRNA pairs, or the low Bxb1 efficiency.
Results<br /> Figure 2:<br /> The figure demonstrates twinPE’s efficiency in large DNA sequence insertion and replacement. However, the formatting is poor, the figure legend is separate from the figure and labels are a bit confusing. The authors should revise the figure to improve readability.<br /> The large error bar in Fig. 2F (deletion size 589) suggests variability in the editing strategy. The authors should address this in the text, discussing potential outliers or variability in the system.
Figure 3:<br /> This figure effectively shows the mechanism and efficiency of twinPE combined with Bxb1 integrase. However, the authors should clarify why certain pegRNA pairs performed better than others and why some loci (e.g., CCR5, AAVS1) were more successful.<br /> The discussion should also address the limitations of single transfection compared to sequential transfection to allow researchers to build off of this work.
Figure 4:<br /> The figure explores therapeutic applications of twinPE, particularly in correcting inversions at recombination hotspots. The authors should expand on the implications of these findings for gene therapy and discuss potential challenges in scaling up for human applications.
Discussion<br /> The discussion is well-written but could be strengthened by addressing the following:<br /> Limitations of twinPE: The authors should discuss why lower frequencies occurred in single transfection compared to sequential transfection and why some pegRNA pairs performed better than others. Additionally, they should explore the potential limitations of using Bxb1 integrase and whether other integrases could be more effective.<br /> Comparison with other gene-editing techniques: The authors briefly mention the advantages of twinPE over CRISPR but do not provide a direct comparison. Including experimental data or a discussion comparing twinPE to CRISPR or other editing methods would strengthen the paper.<br /> Long-term implications: The study lacks long-term data on genomic stability after large DNA modifications. The authors should discuss potential risks, such as off-target effects or genomic instability, and suggest future studies to address these concerns.
Suggestions<br /> Improve Figure Quality: Revise figures to ensure they are clear, readable, and properly formatted. Include detailed legends and consider adding summary panels to highlight key findings.<br /> Expand on Limitations: Discuss the limitations of twinPE in more detail, including variability in editing efficiency, challenges in scaling up for human applications, and potential long-term effects on genomic stability.<br /> Compare with Other Techniques: Include a direct comparison of twinPE with CRISPR or other gene-editing methods to highlight its advantages and disadvantages.<br /> Explore Additional Integrases: Investigate the use of other integrases in combination with twinPE to determine if they offer improved efficiency or precision.<br /> Provide Long-Term Data: Conduct follow-up studies to assess the long-term effects of large DNA modifications on genomic stability and cell viability.<br /> Enhance the Introduction: Add more background information on the limitations of existing gene-editing technologies and how twinPE addresses these challenges.<br /> Address Variability in Results: Discuss potential outliers or variability in the data, particularly in Fig. 2F, and suggest ways to improve consistency in future experiments.
Editorial Decision<br /> The paper presents significant advancements in gene-editing technology and demonstrates the potential of twinPE for precise and efficient large DNA sequence modifications. However, the study would benefit from addressing the limitations and expanding on the comparisons with other gene-editing techniques. This publication could be strengthened with revisions to improve figure quality, clarify data interpretation, and exploring long-term stability the genetic edits. Overall, the paper was dense with information so the limitations are understandable, as only so much can be presented in one publication.
On 2025-02-26 09:56:55, user Jonathan Rondeau-Leclaire wrote:
was looking forward to that preprint (saw your talk at cshl microbiome!)
quick suggestion for figure 5: use a horizontal jitter so we can distinguish points that fully overlap (e.g. both VAMB in panel b. seem to be perfectly overlapping, but we can't be sure)
best of lucks for publication!
On 2025-02-25 21:24:18, user Xiaotong Yao wrote:
The measurements for the "realistic"-ness of the simulated genomes seems inadequate. For examples, what are the VAFs of mutations in the LOH or homozygously deleted or amplified regions?
On 2025-02-25 21:16:36, user Xiaotong Yao wrote:
No. You simply cannot "simulate" structural variants as if they are just rows in a BEDPE file.
Doing it in the way of this paper won't even guarantee your CNV boundaries are matched correctly with the junction breakends! Let alone consistent junction copy numbers or realistic complex SV events. This approach of treating each "variant" as an individual event only works for short variants, and CNVs to some extent.
To truly forward simulate a cancer genome that is accumulating structural variants/CNVs requires virtual cell cycles and keeping tabs on the junction balance constraints and linear/circular DNA structures, e.g., losing a telomere, di-centric chromsomes. We tried this before, but it is very very hard as the genomes coming out of the simulations are not anything remotely survivable for a cell and nothing like the real cancer genomes. So this is a fascinating and challenging open question.
On 2025-02-25 05:38:33, user Roberto Nava wrote:
The reporter system is genius! Any chance the authors would be willing to share the supplemental tables? They don't appear in the PDF.
On 2025-02-25 01:58:05, user Maria Rebolleda Gomez wrote:
Really interesting paper showing that variation across strains in the relationship between growth rate and antibiotic-induced lysis as well as interactions can shape the outcomes of community re-structuring after antibiotic treatment. The authors are able to use data from individual E. coli strains to predict the overall enrichment in the community after antibiotics. However, the last step of the derivation in the methods was not clear to me why is it G_m,i + C - It is not clear what that constant is. Also in the main body of the paper it states that this is an approximation, but in the derivation is stated as an identity relationship.
On 2025-02-25 00:16:29, user Meet Zandawala wrote:
This study investigates the dynamics of neuropeptide release and activity following blood feeding in female Aedes aegypti mosquitoes. Sajadi et al. provide valuable insights into the temporal signaling dynamics of diuretic and anti-diuretic hormones, significantly enhancing our understanding of excretory physiology in mosquitoes. The authors employ heterologous expression of receptors to quantify circulating peptide levels, a robust methodological approach that strengthens receptor-ligand interaction validation and hormone quantification. Notably, the study demonstrates a synergistic interaction between DH31 and kinin-like peptides on Malpighian tubules, contributing novel findings to the existing literature on neuropeptide-mediated excretory regulation in mosquitoes. Overall, the study presents an innovative and well-executed investigation with high methodological rigor.
The authors have presented their findings in a clear and well-structured manner. We only have a few questions and comments/suggestions that could help improve the clarity of the manuscript:<br /> 1. Can the authors clarify the exact number of female mosquitoes used in each condition (blood-fed vs. non-blood-fed) at each time point, specifically in methodology section 3.2 for the haemolymph collection?<br /> 2. Were there any biological replicates across different mosquito cohorts? Did the authors observe variability between different mosquito batches? Sample sizes have been provided in the figure captions but what does n signify? <br /> 3. The study utilizes specific time points for haemolymph collection post-blood feeding. Can the authors provide justification for selecting these intervals? Were preliminary studies conducted to determine these as the most informative time-points, or were they based on prior literature?<br /> 4. The authors acknowledge the roles of serotonin (5HT) and DH44 in regulating fluid secretion but focus their experimental analysis on DH31, kinin, and CAPA peptides. Could they clarify why 5HT and DH44 were not included in their haemolymph quantification assays? Were there methodological limitations, or were these hormones not expected to show significant post-bloodmeal changes, or is this something they plan to address in the future?<br /> 5. The study quantifies neuropeptide levels over time but does not discuss the mechanisms responsible for their clearance from haemolymph. Can the authors speculate on whether DH31, kinin, and CAPA peptides are degraded enzymatically, removed through receptor-mediated internalization, or cleared by the Malpighian tubules? Can they use in silico approaches to predict the half-life of these peptides based on their sequence composition? Alternatively, can they extract hemolymph when the peptide has peak activity and test this extract after different times to see how much bioactivity they retain over time? Addressing this would enhance our understanding of neuropeptide turnover and regulation.<br /> 6. Including the individual data points in the bar graphs can provide more information on the spread of the data.
Comments prepared by Bilal Amir (on behalf of Zandawala lab)
On 2025-02-24 11:41:36, user Peer wrote:
Hello,<br /> I know it's not 100% necessary to mention this in your paper, but through what kind of screen did you identify ISIC1/2 and STIR1/2? <br /> Thx:)
On 2025-02-24 03:43:01, user ryhisner wrote:
I am unable to copy and paste anything into the reference window in the variability tab. It only allows me to type, not copy and paste. This means I would have to type in the entire nucleotide sequence by hand, which I'd rather not do.
On 2025-02-24 01:16:55, user Alex Monell wrote:
Hi bioRxiv staff,
The published version of this manuscript is out at https://www.nature.com/articles/s41586-024-08466-x
Thanks!
On 2025-02-23 17:35:21, user Sean Rands wrote:
This work was published last year in Open Biology -- see https://doi.org/10.1098/rsob.230430
On 2025-02-23 17:33:44, user Sean Rands wrote:
This work was published last year in Royal Society Open Science - see https://doi.org/10.1098/rsos.231882
On 2025-02-23 10:16:14, user Christian Wunder wrote:
Available on NCB:
On 2025-02-23 02:33:22, user Cecil Saunders wrote:
I believe there is a typo in the abstract citation; Charles, 2019 should be Darwin, 2019.
On 2025-02-21 20:37:42, user Krzysztof Kozak wrote:
Multiple technological choices resulted in fatal flaws that make the conclusions of this manuscript unjustifiable:<br /> 1. Inadequate chain of custody of the samples, likely leading to massive contamination.<br /> 2. Application of insufficient sequencing methods and inappropriate data processing tools, potentially resulting in various technical artefacts.<br /> 3. Lack of replication, further exacerbated by deliberate mixing of the isolates.<br /> 4. A simplistic and biased interpretation of the observed patterns of change in the molecular sequences.
I posted a full review of the paper on ResearchHub: https://www.researchhub.com/paper/9161412/discovery-of-single-stranded-dna-in-meteorite-derived-cultures-evidence-of-novel-genetic-elements/reviews
On 2025-02-21 15:30:18, user Yuan Fu wrote:
The paper was published in JIPB on February 21, 2025. The DOI link is: https://doi.org/10.1111/jipb.13867 . Please cite it.
On 2025-02-21 14:20:17, user JJ wrote:
In figure 2, part D, the figure legend says - "The median UMI/gene count is shown as a number above a dataset and as a bold line". Does the numbers say UMI/gene or is it just the Median Number of Genes for each dataset?
On 2025-02-21 11:30:52, user mcsu wrote:
Hi, <br /> Care must be taken when using old data tables for example in table S1 the uniprot_IDs given for the following U. maydis proteins no longer map:-<br /> PRA1_USTMA <br /> PRA2_USTMD <br /> UM03423
but are <br /> P31302<br /> P31303<br /> A0A0D1E0T5
In addition, given these errors how confident are you that the Literature-sourced GPCRs are classified correctly?<br /> Many of the Pfam domains claimed to be "consistent with their associated GPCR class (Table 1)" are not found in the exemplar sequences of each class in table S1.<br /> For example, the Git3 Pfam PF11710 suggested as associated with CPCR class 3 is only found in GPR1_YEAST and not the other 4 proteins suggested as Class 3 GPCRs in table S1; see A0A1U8QVN2_EMENI, A0A1U8QIJ6_EMENI, A0A1U8QJM4_EMENI or Q7SAB9_NEUCR
On 2025-02-21 09:14:43, user Wenjun wrote:
Great work! In addition to enhancing light collection efficiency, the proposed method also effectively reduces the number of optical components in the remote imaging system.
On 2025-02-21 09:00:55, user Froy wrote:
A pity this citation is missing: https://www.cell.com/cell-reports/fulltext/S2211-1247(22)00444-2
On 2025-02-21 01:11:53, user Charles Warden wrote:
Thank you very much for posting this preprint for the Giotto Suite!
You have a couple different citations for STalign.
I believe this is the correct citation (Reference 34):
34.↵Clifton, K. et al. Alignment of spatial transcriptomics data using diffeomorphic metric mapping. BioRxiv Prepr. Serv. Biol. 2023.04.11.534630 (2023) doi:10.1101/2023.04.11.534630.Abstract/FREE Full TextGoogle Scholar
However, I think the following reference (to Hildebrandt et al. 2021) may not be correct?
"Image registration was performed using STalign [Reference 2]"
Best Wishes,<br /> Charles
On 2025-02-21 00:46:47, user Hurrian Fan wrote:
Congratulations to the team on some amazing work! The steppe component visible in East_steppe_Sets in Chalcolithic and Bronze Age western Anatolia is modeled with Yamnaya, CWC, and Bell Beaker, which are chronologically and geographically somewhat improbable for the early samples. <br /> Have the authors considered checking potentially more proximal sources of potential steppe ancestry, such as the Kartal A & B clusters from Penske et al 2023?
The subclades of y-hg I-L699 found in the Kulluoba and Kalehoyuk samples are not only shared with Serednii Stih individuals, but also Cernavoda (KTL001 & KTL006) and Thracian EBA individuals (Bul4 & I2165), which might lend some plausibility to this source.
On 2025-02-20 20:30:48, user Jesse Conklin wrote:
This should be linked to the final publication:
Conklin, J. R., Verkuil, Y. I., Lefebvre, M. J. M., Battley, P. F., Bom, R. A., Gill, R. E. Jr, Hassell, C. J., ten Horn, J., Ruthrauff, D. R., Tibbitts, T. L., Tomkovich, P. S., Warnock, N., Piersma, T., & Fontaine, M. C. (2024). High dispersal ability versus migratory traditions: Fine-scale population structure and post-glacial colonisation in bar-tailed godwits. Molecular Ecology, 33, e17452. https://doi.org/10.1111/mec.17452
On 2025-02-20 19:02:49, user Raoul wrote:
There is a previous report that has targeted a disease resistance gene to generate plants with enhance resistance. Similar to what is said in this pre-print ("SNC1 is an attractive target for proof-of-principle modulation of disease resistance by epigenome engineering").<br /> Reference: CRISPRa-mediated transcriptional activation of the SlPR-1 gene in edited tomato plants<br /> Plant Sci, 329 (2023), Article 111617, 10.1016/j.plantsci.2023.111617<br /> Recently a review article has mentioned that: "One notable example of enhancing disease resistance in crops involved the CRISPR activation (CRISPRa) system to activate the defense gene PATHOGENESIS-RELATED GENE 1 gene (SlPR-1) conferring enhanced resistance to Clavibacter michiganensis subsp. michiganensis infection in tomatoes" (taken from: https://doi.org/10.1016/j.pbi.2024.102669 ).<br /> Consequently, the concept has shown to be scientifically and technically feasible, as shown previously in 10.1016/j.plantsci.2023.111617.<br /> Thus, what is stated in this preprint is not really new, for plants: "The results demonstrate that epigenome-engineering of a single defense gene, SNC1, is sufficient to generate plants with improved disease resistance phenotypes."
On 2025-02-20 14:08:04, user Prashant Kaushik wrote:
Could the author kindly comment on how human plasma was processed post collection? Were there sequential centrifugation steps involved and were they consistent among different MS based tech? <br /> Thank you for sharing your fantastic Work
On 2025-02-20 13:55:28, user andy wrote:
Dont forget Bdellovibrio has deacetylases - comment on statement in manuscript about lack of these in Gram negatives
On 2025-02-20 12:15:37, user kei wrote:
Thank you for your interesting paper.
I am curious about the behavior when only the non-natural amino acids in cyclic peptides are not tokenized at the atomic level, and all cyclic peptides are represented using SMILES. I am thinking of investigating this.
That said, I have one question:<br /> What is the input format when inferring complexes of cyclic peptides containing non-natural amino acids and proteins?<br /> (In other words, how are non-natural amino acids formatted in the input?)
If possible, I would appreciate it if you could share an example of the YAML file or other input data used for Boltz1.
Thank you in advance.
On 2025-02-19 13:17:06, user Ali Ryan wrote:
MdaB is not a membrane associated quinone reductase as suggested in figure 5a, it is homodimeric and cytosolic as far as anyone has characterised.
On 2025-02-19 03:28:56, user Yue Jia-Xing wrote:
Author comment:<br /> This work has been formally published in Genome Research recently under a different title:<br /> "Interactive visualization and interpretation of pangenome graphs by linear reference–based coordinate projection and annotation integration".<br /> Advanced online on 2025.01.13, formal publication in 2025.02.<br /> DOI: 10.1101/gr.279461.124 <br /> Link: https://genome.cshlp.org/content/35/2/296.full
On 2025-02-18 17:40:04, user Dongyao Li wrote:
Great work, thank you! I have one comment regarding comparison of cell segmentation. The paper states:
Overall, the CosMx 6K segmentation tool produced cells with larger sizes, higher solidity, and better circularity, indicative of more regular and convex cell shapes compared to other platforms
I would argue "larger", "more circular", and "convex" do not necessarily mean better segmentation. For example, "more circular" and "convex" could be the bias of the particular segmentation model. If more circular is better, then "nucleus segmentation + large expansion" (basically the first version of Xenium segmentation prior to multi modal cell segmentation stain) is the better segmentation since it's large, circular, and convex.
The paper later states:
Among the ST platforms, Xenium 5K showed better separation of marker gene pairs after segmentation
We further visualized marker gene expression across the annotated cell types. Xenium 5K exhibited the most distinct expression patterns (Supplementary Fig. 8d), facilitating more accurate cell type annotations.
and concludes:
Despite exhibiting more irregular segmentation shapes, Xenium 5K effectively distinguished different cell types and minimized transcript mixing between adjacent cells
"Better separation of marker gene pairs", "distinguish different cell types" and "minimize transcript mixing" are indeed the more principled and biologically meaningful metrics to evaluate cell segmentation. The word "despite" in the conclusion suggests circularity means better segmentation, which I don't necessarily agree.
On 2025-02-18 15:37:48, user Andrew Kennard wrote:
This preprint has since been peer-reviewed, revised, and published in a journal:
Kennard AS et al. (2025). Tubulin sequence divergence is associated with the use of distinct microtubule regulators. Current Biology 35(2): p233-248.e8. doi: https://doi.org/10.1016/j.cub.2024.11.022
On 2025-02-17 21:53:40, user Alessandro Hernández wrote:
Are you thinking on use this tool for alleles that has been under natural selection? For example LCT (lactase persistance allele) which are very common in european populations and some parts of Africa. Do you hypothesize that they could be restricted to certain populations and obtain an ADS >0?
On 2025-02-17 18:48:35, user Michael Young wrote:
We just discussed this paper in our lab - nice work! One minor comment and one general one. Figure 2f - use same x-axis for both plots. More importantly, the paper is trying to do a lot. Not sure whether we would suggest splitting into two papers, relegating some elements to supplementary materials, or keeping as is with details relegated to supplementary.
On 2025-02-17 08:16:49, user Jeziel Dener Damasceno wrote:
Please, could this preprint be linked to the final publication, please: https://www.nature.com/articles/s41467-025-56785-y
On 2025-02-16 01:30:11, user Nikolai Slavov wrote:
Code and data for reproducing the analysis are available at: <br /> https://github.com/SlavovLab/Protein-Clearance
On 2025-02-15 17:23:55, user Maxwell Neal wrote:
A peer-reviewed version of this manuscript has been published at https://doi.org/10.1093/bioinformatics/btae442
On 2025-02-15 03:06:45, user Jayson Zhao wrote:
how about the nearest neighbor search algorithm behind that strongly affect the loss function of non-linear dimension reduction and dataset dimension, in which we will have hubs. See some discussion here: https://academic.oup.com/nargab/article/6/4/lqae172/7928174
On 2025-02-15 02:39:09, user sa pa wrote:
I read this paper with great interest.
Is there a name given to the single-cell RNA-seq using the “Solution-phase indexing by kinetic confinement” technique that you are proposing?
It would be easier to cite it as a single-cell RNA-seq method if it had a name like “xxx-seq”, but what should we call it officially?
In the text, it says “Single cell RNAseq using Kinetic Confinement”, is this correct?
On 2025-02-14 04:28:23, user Felix wrote:
I have only skimmed the paper, but I wonder if the link given for the fungal catalogue ( https://entrepot.recherche.data.gouv.fr/dataset.xhtml?persistentId=doi:10.15454/WQ4UTV ) is the correct one. It redirects to human oral microbiota gene and species catalogue rather than fungal-specific catalogue.
On a somewhat related topic, have the authors considered expanding the fungal catalogue with the recent cultivated human gut fungi resource ( https://doi.org/10.1016/j.cell.2024.04.043 )?
On 2025-02-13 22:20:55, user Amer Alam wrote:
The peer reviewed version of this manuscript has been published in the EMBO journal:
Structural insights into binding-site access and ligand recognition by human ABCB1
PMID: 39806099 DOI: 10.1038/s44318-025-00361-z
On 2025-02-13 19:40:38, user Pick Up Litter wrote:
This paper will help move science away from studying "cute" species and to be objective. Perhaps the most severe example is the housecat-- still portrayed as cute in media, but in the feral form a worldwide destroyer of birds. One critique concerning the Ivory-billed Woodpecker-- the number quoted by Troy et al, 20 million dollars spent for studies, is misleading. Most of the efforts are university and private, not governmental, and if the bird is proven to be extant, will have conservation benefits since it is a wide-ranging and keystone species. I help with research for the Ivory-billed Woodpecker. The growing body of evidence that this species exists is more rational than the critique-- see other BioRxiv papers and the work of Mike Collins for example. John D Williams
On 2025-02-13 17:59:30, user Mikaela Gray wrote:
This preprint has now been published in ACS Omega. Here is the link: https://pubs.acs.org/doi/10.1021/acsomega.4c07666
On 2025-02-13 15:16:40, user XUAN ZHANG wrote:
Now published in Cell: https://www.cell.com/cell/fulltext/S0092-8674(24)01273-X
On 2025-02-12 14:36:44, user Sergio Angel wrote:
Very interesting. Our anti-TgATM antibody also labeled the cytosol, with phleomycin in cytosol and some foci in nucleus.
On 2025-02-12 10:42:04, user Claudio Vasapollo wrote:
This manuscript has been published with a different title wanted by the journal. You can find the published version on the PeerJ website at the link:<br /> https://peerj.com/articles/18765/
Thank you.<br /> Claudio Vasapollo
On 2025-02-12 06:12:29, user Prof. Sergio Manni Vanzini wrote:
The paper presents a novel perspective on the application of oxygen-ozone therapy in spine disorders, introducing the concept of adaptive chaos as a key mechanism in biological resilience and healing. A significant strength lies in its interdisciplinary approach, integrating mathematical modeling, bioinformatics, and clinical insights to establish a framework for understanding the therapeutic effects of ozone therapy. The use of Lyapunov exponents, Shannon entropy, and fractal dimensions to quantify biological complexity is particularly innovative, providing a structured means of evaluating systemic responses to treatment. Additionally, the study’s emphasis on precision dosing—highlighting the differential effects of low versus high ozone concentrations—adds valuable insight into the hormetic nature of the therapy, reinforcing the need for controlled perturbations in medical interventions. The thorough review of existing literature, including randomized controlled trials, strengthens the credibility of the findings and underscores the translational potential of the proposed model.<br /> However, certain limitations must be acknowledged. The reliance on mathematical simulations, while insightful, may not fully capture the variability of real-world biological responses, as complex physiological interactions are difficult to model with absolute accuracy. Additionally, while the study references clinical data, it does not provide direct experimental validation, making it difficult to assess the immediate applicability of the findings in clinical practice. The concept of adaptive chaos, though compelling, remains somewhat abstract, and further empirical studies are needed to establish its clinical relevance definitively. Lastly, some of the statistical approaches, particularly the unusually high values of Lyapunov exponents, may require re-evaluation to ensure their biological plausibility and proper contextualization within established dynamical system theory. Despite these challenges, the study provides a groundbreaking theoretical framework with promising implications for regenerative medicine and personalized therapy.
On 2025-02-10 12:29:07, user Alberto Farleschi wrote:
I came through these data, which represents a novelty for me, endeavoured in the field of bioinformatics. The study by Chirumbolo et al. presents a compelling and innovative perspective on adaptive chaos and its role in modulating oxygen-ozone therapy for spine disorders. By integrating mathematical modeling, bioinformatics, and clinical insights, the authors provide a rigorous framework to understand how mild chaotic perturbations can enhance systemic complexity and biological resilience.<br /> A particular strength of this work lies in its multidimensional approach, incorporating Shannon entropy, Lyapunov exponents, and fractal dimensions to quantify the therapeutic impact of oxygen-ozone therapy. Therefire, in my opinion, the authors successfully demonstrate that low-dose ozone (20–40 µg/ml O3) fosters adaptive chaos, leading to reduced inflammation, enhanced repair, and improved systemic stability. In contrast, higher doses (>60 µg/ml O3) appear to push the system into pathological chaos, emphasizing the importance of precision dosing in regenerative medicine. Really interesting outcomes!<br /> The translational significance of this study cannot be overstated. It not only advances our understanding of chaos-driven medical interventions but also sets a precedent for personalized medicine strategies that leverage nonlinear dynamics to optimize therapeutic outcomes. Future research could expand on these findings by incorporating real-world clinical datasets and patient-specific modeling, further solidifying the role of adaptive chaos in medical practice.<br /> I trust this study is a landmark contribution to the fields of biophysics, complexity science, and regenerative medicine, offering novel insights into the interplay between biological chaos and therapeutic control.<br /> Great results!!
On 2025-02-11 09:45:35, user Jianhua Xing wrote:
Some movies do not show up. Before I upload a revised version, one can download them here<br /> https://drive.google.com/file/d/1tgdOd6X_d5oRtmamBrLf-TOA8T52xft1/view?usp=sharing
On 2025-02-10 16:30:17, user Pierre L wrote:
last references are not present in the article.
On 2025-02-10 16:19:15, user David Lähnemann wrote:
At the time of writing, the GitHub repository simply gives a 404 This is not the web page you are looking for at:<br />
https://github.com/wbvguo/BSReadSim.git <br />
Did you forget to make the repo public? Or is there a typo in there somewhere?
On 2025-02-10 12:31:19, user Caroline Fernandes Dos Santos wrote:
Published version: https://doi.org/10.1590/0001-3765202520240363
On 2025-02-10 11:32:39, user malandrin wrote:
The prepint is now published in Ticks and Tick Borne Diseases DOI10.1016/j.ttbdis.2024.102434.
On 2025-02-10 11:10:36, user Siobhán McClean wrote:
This article is now published in Microbiology Open. The citation is as follows:
Dennehy, R., Duggan, N., Dignam, S., McCormack, S., Dillon, E., Molony, J., ... & McClean, S. (2022). Protein with negative surface charge distribution, Bnr1, shows characteristics of a DNA‐mimic protein and may be involved in the adaptation of Burkholderia cenocepacia. MicrobiologyOpen, 11(1), e1264.
On 2025-02-09 11:10:57, user Zheng Gong wrote:
The authors should note that in line 549, the promoter that drives gRNA expression is the U6 snoRNA promoter and not a "Ubiquitin 6" promoter. Otherwise, a very interesting read!
Thank you!
On 2025-02-07 23:35:18, user Prof. T. K. Wood wrote:
On 2025-02-07 21:55:49, user Patricia Legler wrote:
We made FRET substrates for CHIKV PMID: 30742841. They are in the Suppl. Info.
On 2025-02-06 17:30:29, user John LaCava wrote:
This is now published at Mobile DNA: https://mobilednajournal.biomedcentral.com/articles/10.1186/s13100-024-00339-4
On 2025-02-06 16:55:23, user Max wrote:
It would be really interesting to see a network of sample relatedness plotted geographically. Maybe this would reveal some interesting trends that are masked by only analyzing spatial distance.
On 2025-02-06 12:27:20, user Prof. T. K. Wood wrote:
page 51: CRISPR-Cas type IE is NOT inactive as found by at least two groups. It has been shown to control the cryptic prophages ( https://www.mdpi.com/1422-0067/23/24/16195 ).
On 2025-02-06 06:08:45, user Jubin Rodriguez wrote:
Why use words such as "we" and "our" when there is only study author?
On 2025-02-06 02:55:28, user Tom Liang wrote:
Excellent contribution to understanding the microscopic mechanisms of anion transport across Band 3! I would like to draw the author’s attention to a highly relevant recent publication in Langmuir: https://doi.org/10.1021/acs.langmuir.4c00216
On 2025-02-05 23:24:58, user Emry Gutierrez wrote:
Great paper! I was curious on the procedures regarding preparing the 48 well plates, as we've been trying to implement these methods into our experiments. Who can I reach out to for more information?
On 2025-02-05 17:50:10, user Emry Gutierrez wrote:
Great paper! Would any of the authors be able to share their procedures for preparing the 48 well plates? We've been trying to implement this methodology and this has been causing us some difficulties!
On 2025-02-05 21:55:34, user Evan Saitta wrote:
This preprint has been formally published:<br /> https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0298957
On 2025-02-05 21:52:46, user Evan Saitta wrote:
This preprint has now been formally published:<br /> https://www.sciencedirect.com/science/article/pii/S0016703723005781
On 2025-02-05 21:51:35, user Evan Saitta wrote:
This preprint has now been formally published: https://elifesciences.org/articles/46205
On 2025-02-05 17:26:07, user Star pupil wrote:
There are other cysteineless interns reported to be equally fast if not faster https://www.lens.org/lens/patent/129-790-217-267-302
On 2025-02-05 16:27:18, user anonymous wrote:
"Not previously reported as a direct USP7 substrate, ..." - this may not be entirely accurate; to my knowledge, Liu et al. (2024) may have demonstrated this in their study.
On 2025-02-05 14:46:01, user Prof. T. K. Wood wrote:
First paragraph is misleading as toxin/antitoxin systems have known to inhibit phage for almost 3 decades so instead of citing a review, the original seminal report should be cite: doi: 10.1128/jb.178.7.2044-2050.1996
On 2025-02-05 10:44:20, user pablo RANEA ROBLES wrote:
Hi! This is a very interesting study, and very relevant considering the debate on omega-6 PUFAs on metabolic health. However, when we were going to read it for a journal club we missed the methods section on this preprint.