RT @joe_pickrell: Interesting study on sex chromosome trisomies and their phenotypic impacts using large biobanks Prevalence of sex chromo…

RT @LippertChr: Turns out LLM embeddings of OMOP concepts provide better transfer between different EHR databases than the OMOP exchange st…

Project led by Matthias Kirchler, Matteo Ferro and @LippertChr. Using resources from @uk_biobank @FinnGen_FI @FIMM_UH @MountSinaiNYC Preprint link:

RT @eshg_young: Got summer plans?☀️ How about diving into cutting-edge human #genomics?🧬 ✨Apply for the Leena Peltonen School of Human Geno…

RT @pnatarajanmd: @MariosGeorgakis Need new ways to enrich for CV events to improve the efficiency of secondary prevention RCTs with contem…

RT @eshgsociety: The deadline to submit your abstract for #eshg2025 Conference is fast approaching. Do not miss the opportunity and submit…

RT @dr_appie: Our first multi-national GWAS on income is out in @NatureHumBehav 🧬💰 - 162 loci (88 novel) - significant heterogeneity betw…

RT @BrentRichards19: Here we describe the role of endotrophin in cardiovascular disease. Great work from @SatoshiYoshiji and others. h…

RT @mendel_random: Looking forward to @MoritzGerstung seminar on “Using AI to predict disease risks” @mrc_ieu on the 30th Jan 2025 at 1pm,…

@C_Glastonbury yes. at least for gene hunting.

RT @PS_cryoEM: Excited to see the first batch of biomass safely delivered from our National Facility for Structural Biology @humantechnopol…

@doctorveera Exciting! Although i’m thinking:How they can have 120M de-identified EHR data but still go back to patients and ask for consent for genetic? I’m always amazed how “flexible” is the use of sensitive health data in US. As always, good and bad aspects

RT @doctorveera: RGC to sequence 10 million participants through collaboration with Truveta! RGC is building the world's largest genetic da…

RT @hrushikesh_loya: (1/6) Excited to share our manuscript describing Quickdraws, a novel algorithm and software to perform GWAS that incre…