Arthur Gilly retweeted
A first deep whole genome sequence-based look at 257 circulating protein biomarkers: novel common and rare variant pQTLs, polygenic risk score prediction and causal links to disease. All in a day’s work for @ArthurGilly :)
Whole genome sequencing analysis of the cardiometabolic proteome biorxiv.org/content/10.1101/… @EleZeggini
Arthur Gilly retweeted
Population-wide copy number variation calling using variant call format files from 6,898 individuals biorxiv.org/cgi/content/shor… #biorxiv_bioinfo
Arthur Gilly retweeted
Cohort-wide deep whole genome sequencing and the allelic architecture of complex traits - new article from @EleZeggini and @ArthurGilly
now online at @NatureComms nature.com/articles/s41467-0…
Arthur Gilly retweeted
A universal SNP and small-indel variant caller using deep neural networks go.nature.com/2NBuDgX #machinelearning
Arthur Gilly retweeted
A one penny imputed genome from next generation reference panels biorxiv.org/content/early/20…
Arthur Gilly retweeted
Large-scale whole-genome sequencing of three diverse Asian populations in Singapore biorxiv.org/cgi/content/shor… #bioRxiv
Arthur Gilly retweeted
Our latest on @biorxivpreprint 1.3M GWAS for insomnia - terrific job @phi_jan, with the #CTGlab team, @23andMeResearch and others! bit.ly/2Er4pGa
Arthur Gilly retweeted
Posthuma introduces FUMA, a tool for fxnl annotation of #GWAS summary stat data fuma.ctglab.nl #neurogen17
