Jason Yang (@JasonJuechen) profile picture

BMI PhD student @ University of Cincinnati, Cincinnati Children’s Hospital Medical Center

Cincinnati, OH
Joined December 2013
🎉 Thrilled to share that my first-author paper as a PhD student is officially in Cancer Discovery now: doi.org/10.1158/2159-8290.CD… Huge thanks to my mentors for their invaluable guidance, and to all my amazing collaborators for their support and insights throughout this journey.
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Copper drives remodeling of metabolic state and progression of clear cell renal cell carcinoma biorxiv.org/cgi/content/shor… #biorxiv_cancer
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Jason Yang retweeted
Our recent work on COVID-19 single cell meta-analysis using ToppCell. biorxiv.org/cgi/content/shor… Welcome to play with the data on ToppCell COVID-19 signature atlas on toppcell.cchmc.org/biosystem…
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Happy to share our latest computational tool -- scTriangulate, leveraging cooperative game theory to mix-and-match diverse cluster boundaries to achieve the optimal clustering results! (1/n)biorxiv.org/content/10.1101/…
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Jason Yang retweeted
ATAC peak calling with MACS2: I know this is a recurring problem but I got asked a few times recently, so I just put all info here for my own ref. We now routinely convert paired BAM to simple BED file and use "-f BED --shift -100 --extsize 200" for the peak calling. Why? 1/7
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Very nice overview: Tutorial: guidelines for the computational analysis of single-cell RNA sequencing data. nature.com/articles/s41596-0…
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Replying to @tangming2005
Have you checked out bio.tools that's a cool resource offered by embl provides link outs to publications using the tool and altmetrics.
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there are so many genome fasta and gtf files available from different resources: UCSC, Ensembl, genecode. which files are recommended for RNAseq and DNAseq alignment? Heng's post answered some of it lh3.github.io/2017/11/13/whi… what about gtf, gtf should be compatible with fasta
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