To promote the rapid dissemination of new research, bioRxiv and medRxiv depend on Affiliates who help screen manuscripts. Affiliates are active scientists who volunteer their time to quickly determine whether submitted articles include biological research and do not have the potential to cause harm to the public. Marc Robinson-Rechavi has been a bioRxiv Affiliate since 2021. Marc is a Professor of Bioinformatics at the University of Lausanne and his research is focused on linking the evolution of animal development to genome evolution.? Marc enjoys being an affiliate so that he can help make the promise of preprints a reality and, since becoming one, he has learned how the sausage of preprinting is made and what a wonderful community of people are behind biorXiv. Thanks to affiliates like Marc we can continue sharing new research within ~48h of submission. To learn more about our screening procedures please click here: https://lnkd.in/e_9MkmBb
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?????????? ?????? ?????????? ?? ???????????????? ?????? ???????????????? ???????????? ?????????????????????? Join global experts to share best practices for clinical genomics and data sharing! ??? ??????????: ????- ???? ???????? ???????? ?????? ???????? ?????????????? ???? ???????????? ?????? ????????: #CCG25 This hybrid conference will unite the global clinical genomics and biodata communities to establish common standards, best practices, and integrate recent research to drive improvements in patient care. Bursary support will be available for anyone facing financial barriers to attending research meetings. ?? ?? ?????????? ???? ???????? ?????? ???????? ?????????? ???????? ?????????????? ???? ?????? ??????????????: https://bit.ly/4hz5zkS There will be multiple opportunities to share your own work as either a short talk or poster presentation, once the conference opens to accept registrations. National Human Genome Research Institute (NHGRI) | European Bioinformatics Institute | EMBL-EBI | The Francis Crick Institute | Wellcome Sanger Institute #AcademicChatter #PhDChat #PhDLife #ResearchMeetings #ClinicalGenome #Genomics #ClinicalGenomics #VariantInterpretation #GenomeVariation #BigData
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"Advancing my skills in bioinformatics and genomics, I've successfully completed a month-long online workshop on Genomes, Networks, and Pathways. Ongoing education fuels my passion for innovation." With Decode Life #Genomics #NetworkBiology #PathwayAnalysis #OnlineWorkshop #InternationalCollaboration #ProfessionalDevelopment #Bioinformatics
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"Are you diving into the fascinating world of bioinformatics? ?? Check out this list of the Top 10 Must-Read Research Papers that have shaped the field!?? Which of these papers had the biggest impact on the field? Or is there a favorite paper that isn't on this list? Let’s discuss below! ?? #Bioinformatics #ScienceInnovation #ResearchHighlights #Genomics #Proteomics"
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I remember being frustrated as a graduate student, by a protein expression system that simply would not work. Turns out the taq polymerase we were using was introducing a singe base change that turned a tryptophan into a stop codon. Having worked with numerous expression vectors, AAV and mRNA gene therapy systems I can tell you that they are plagued by insertions/deletions/inversions, random mutations and incorporation of adventitious DNA. Since plasmids are the starting point for many downstream biomanufactuing processed they are the obvious best point to focus QC/QA efforts prior to scaling. Nanopore sequencing allows you to capture entire plasmids, ITR-ITR AAV vectors and everything in between on single reads. This gives you a highly accurate, rapid and cost-effective snapshot of total DNA (or RNA) population in a given sample.
Nanopore Account Executive with Oxford Nanopore Technologies - Carrier Screening solutions now available
are you sequencing your entire plasmid?? the data you are missing matters. Serious errors plague DNA tool that’s a workhorse of biology Researchers analysed thousands of laboratory-made plasmids and discovered that nearly half of them had defects, raising questions of experimental reproducibility. https://lnkd.in/gcT26R76
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In Phase 1 of the SCGE program, researchers worked to improve the efficacy and specificity of genome editing approaches. The program has developed a genome editing toolkit to disseminate novel strategies, technologies, and learnings to the broader scientific community. These images highlight some of the different content in the toolkit. Check out this free resource at https://lnkd.in/gUTZFiGJ #genetherapy #genomeediting #science #resource #toolkit
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?? Senior Research Assistant Ashleigh Lister is an expert in the field of #singlecell and spatial #genomics. In this technical article, she shares her insights and first-hand experience of applying #spatialtranscriptomics to non-model plant samples. https://okt.to/3iL8Ea
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A well-preferenced computer is crucial for anyone working in bioinformatics. It enables efficient handling of large datasets, complex computations, and sophisticated analyses… What kind of setup do you have for bioinformatics work? #Bioinformatics #Genomics #ComputationalBiology #Research #TechSetup
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Glad to share my recent participation in a pivotal two-day workshop titled "Role of Bioinformatics in Vaccine Development". This workshop provided an in-depth exploration of how bioinformatics is revolutionizing vaccine research and development. The discussions explored the critical role of genomic data analysis in identifying vaccine targets, the importance of bioinformatics tools in speeding up the vaccine development process, and the future potential of this exciting field in tackling emerging diseases. #bioinformatics #vaccinedevelopment #computationalbiology #genomics #publichealth #innovation #science #research #insilicobiology
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?? Last Chance Alert: 100 Million Cell Challenge Closes Today! ???? The countdown is on! The submission deadline for the groundbreaking 100 Million Cell Challenge is today, October 15, 2024, at 11:59 PM PDT. This is your final opportunity to: ? Access cutting-edge QuantumScale technology ? Potentially receive significant cost subsidies ? Contribute to a project that could reshape single cell genomics research Whether you're working on human tissue, animal models, or other organisms, if your project proposes to analyze 1 million cells or more, we want to hear from you! Don't let this chance slip away. Your project could be the key to unlocking new insights into complex biological systems and driving the future of genomics research. Submit your proposal now: https://hubs.la/Q02TjFGt0 #100MillionCellChallenge #SingleCell #Genomics #LastCall #ResearchOpportunity
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