Paul Gordon
@yycist
Bioinformatician and more
ID: 22634023
https://scholar.google.ca/citations?user=_bNU8kMAAAAJ&hl=en 03-03-2009 15:25:19
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What if you could recombine any two DNA sequences in a programmable manner? We discovered an RNA-guided recombinase that can do just that! So happy to have co-led this project with Nicholas Perry
Did you notice that there was not a Doonesbury in your Sunday Paper (basically any Gannett paper, including the Des Moines Register) here it is! See the thread for all six panels! (1)
The difference in 10x Genomics' Cell Ranger's default between version 6 and 7 is discussed in this thread, but it's such a big deal that it's worth its own thread. tl;dr: in v7 Cell Ranger changed how it produces the gene count matrix leading to a huge difference in results. 1/
Would you believe me if I told you that a single variant in a non-coding RNA explains ~0.5% of all undiagnosed individuals with neurodevelopmental disorders (NDD) in Genomics England ??? I didn’t initially either, but here is the story of RNU4-2 🧵1/9
We're #hiring a #MolecularBiology expert 👨🔬🧪🧬at Ramaciotti Centre for Genomics UNSW Science: Join an amazing team in stunning #Sydney to work with the latest Illumina & Oxford Nanopore workflows and devices. Salary $96k-$103K + 17% super & leave loading. Apply here 👉 shorturl.at/fBISW
Y’all can read about this absolutely distressing situation of me trying to buy a home + learning that the seller didn’t want to sell to me because I’m Black, in The New York Times. Thank you Debra Kamin for your hard work investigating this + educating people about the Fair Housing Act 1/
GitHub update: Tamor, a Snakemake pipeline for Personal Cancer Genome Reports from FASTQ files + Dragen genome/transcriptome analysis, has been updated to work with Sigve Nakken’s 2.0 PCGR system! Now comes with working a public leukaemia data example. GitHub.com/nodrogluap/tam…