Ryan L. Collins, A.B.
NSF Graduate Research Fellow & Ph.D. Candidate
Program in Bioinformatics and Integrative Genomics
Harvard Medical School, Boston, MA
Contact
rlcollins [at] g.harvard.edu
Blog posts by month
- February 2021 (1)
- March 2019 (1)
- June 2017 (1)
- November 2016 (1)
- July 2016 (1)
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@ryanlcollins13
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Interested in complex structural variants and Mendelian diseases? Check out this fascinating example of a dupINVdup causing a blood disorder by @bloodgenes & co 👇 Functional follow-up was crucial to understand the consequence of the SV Glad to have played a (very) small part! t.co/UqcwX5DHjS
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Have your voice heard! We want to hear more about who our users are, how they use gnomAD and what they think we can do to make it better. If you use the gnomAD browser, or download gnomAD data, please take 5 minutes to fill out our user survey t.co/TVeOG5SCfi
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This looks pretty cool. If I read it correctly, they assemble 20% of the genome from one single cell, and can look at things like TCR rearrangement, or identify somatic SVs without the complexity of somatic calling. Impressive this is possible! @_adameur & @infoecho on the work t.co/lpn3rf7Z8i
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👇 Valuable skim for anyone using CRISPR-Cas9 in applications where high edit fidelity is important Not a shocking finding (I assumed outcomes like this were very rare but possible), but hugely important to have this empirically demonstrated! Awesome genome bio here, too👏 t.co/nZyImgodUJ