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NEWS 🎉: All of Us has released its first genomic dataset, which includes whole genome sequences from nearly 100K participants, in addition to genotyping arrays on 165K participants from diverse backgrounds. #Researchers, learn more: bit.ly/3N1vEtO #ResearchAllofUs

Our Community Care Cohort Project (C3PO) paper is out in npj Digital Medicine! C3PO is an #EHR cohort of >500K primary care pts at Mass General Brigham, a powerful resource for #health & #ML research. Broad Institute ML4H Link: go.nature.com/3KqL4pH OG🧵: bit.ly/3juiqYM

Perceptions of #dog breed temperments are ingrained in our culture. Breed #stereotypes play out in dog parks, show up in city ordinances & leases, are celebrated at dog shows, and infuse Hollywood movies... but what if I told you dog temperment doesn't work like that? 1/n

Proud to get this work out into the world! Thanks to everyone who made this possible: Shaan Khurshid Xin Wang RVpacing Daniel Pipilas, MD Jeff Ashburner Patrick Ellinor Daniel Singer @satlas60 @steven_lubitz

Better together. International collaboration gave us the most powerful space telescope ever made, and the deepest infrared views of the universe ever seen. With our partners at @ESA and @CSA_ASC, the science can begin. Together we #UnfoldTheUniverse: go.nasa.gov/3azyGqM

5 websites for drawing scientific figures: 👇 🧵

#ASHG22 Applications of Individual-level Imputed Transcriptomes in the UK Biobank by Xin Wang from Broad Institute working with @steven_lubitz and Patrick Ellinor

Sean Jurgens talking about how sequencing helps us to understand atrial fibrillation with more than 50k cases #AHA2022 Patrick Ellinor James Pirruccello Broad Institute

Great work by Shino Kany presenting genetic substudy of EAST trial this evening at #AHA22 Mass General Heart Broad Institute

A timeless model for writing a good research summary.

#ACC23 YIA / JACC Journals #JACCHF SimPub Problem: ICD codes defining clinical events in EHR / biobanks can be inaccurate We trained/validated a natural language processing model to adjudicate HF hospitalization from d/c summary text jacc.org/doi/10.1016/j.… 🧵

New online from Xin Wang @steven_lubitz + team: Genetic Susceptibility to Atrial Fibrillation Identified via Deep Learning of 12-Lead Electrocardiograms ahajournals.org/doi/10.1161/CI… AHA Science #AHAjournals #CardioTwitter #Genetics 📽️ Video abstract to be posted soon!

#Onthisday 30 years ago, the Sanger Institute opened its doors and started up its sequencing machines to begin working on the Human Genome Project. ⌛️ For #Sangers30th, take a look back at what we have achieved since then ⤵️ sangerinstitute.blog/2023/10/04/30-…

Nature Genetics: Rare coding variant analysis for human diseases across biobanks and ancestries nature.com/articles/s4158… (free: rdcu.be/dSlEf)

Excited to share our recent work on cross-biobank and pan-ancestry genetic analyses of rare variants for human disease 🧬 published last week in Nature Genetics Xin Wang Patrick Ellinor Link: nature.com/articles/s4158…

Very happy and excited to announce that I'll be starting my own research group at EMBL-EBI! The group will focus on lineage tracing, somatic evolution and the origins of cancer. Interested in doing a postdoc in the group or know someone who is? Please reach out!

Nature research paper: Timing and trajectory of BCR::ABL1-driven chronic myeloid leukaemia go.nature.com/4cwdrBS