Introducing the All of Us + AnVIL Imputation Service - Terra
The Broad Institute’s Data Sciences Platform has launched the All of Us + AnVIL Imputation Service. Imputation services allow researchers to leverage large reference panels (without direct access to p...
The Broad's Data Sciences Platform is excited to announce that the All of Us + AnVIL imputation service is now available!
Our reference panel includes 515,000+ genomes, including 250,000+ genomes from non-European inferred genetic ancestries.
Learn more: terra.bio/introducing-...
25.08.2025 16:15 — 👍 1 🔁 1 💬 0 📌 0
Transforming public health and infectious disease surveillance through the innovative implementation of #NGS and #bioinformatics technologies.
Scientist & artist. Prof at UMass Chan Med School & Broad Institute. Rice U alum. Founder of Zoonomia & DarwinsArk.org. Wants your dog’s DNA. And your cat’s! 🇸🇪🇳🇿🇺🇸
GA4GH sets standards and frames policies to expand genomic and health data use within a human rights framework.
https://www.ga4gh.org
Bioinformatics Scientist @theiagen.bsky.social
Likely swimming in a sea of pathogen genomes 🏊🧬 or riding my bike 🚴
Public Health | Infectious Diseases | Bioinformatics | Software Dev
I use genomics to study the evolution and spread of human pathogens and lead pathogen genomic analytics at the Broad Institute.
Also: @dpark@mstdn.science
ORCID: 0000-0001-7226-7781
GitHub: dpark01
Elevating the world through bold and socially responsible innovation. engineering.ucsc.edu #BaskinEngineering
Responsible for instigating some of humanity’s most high-impact discoveries.
Visit us at https://science.ucsc.edu/ 🐋 🔭 🧬
Bloomberg Distinguished Professor at Johns Hopkins University. http://schatz-lab.org
AppSec, Broad Institute, GA4GH, OWASP Boston, Scouting America
Science Communicator in Genomics, Lead Public Affairs at NHGRI, lover of pop culture and romcoms
Revolutionizing genomics with a cloud-powered hub for innovation and collaborative discovery 🚀🧬 #AnVILGenomics
A multidisciplinary community of researchers with the mission to better understand the roots of disease and narrow the gap between new biological insights and impact for patients. Broadinstitute.org
Committed to the daily re-imagining of what a university press can be since 1962.
Website: https://mitpress.mit.edu // The Reader (our home for excerpts, essays, & interviews): https://thereader.mitpress.mit.edu
Genomic medicine researcher; chief genomics officer at MGH; clinical lab director at @broadinstitute
Diverse Human References Drive Genomic Discoveries for Everyone
The GREGoR Consortium (Genomics Research to Elucidate the Genetics of Rare diseases) seeks to develop and apply approaches to discover the cause of currently unexplained rare genetic disorders.
https://gregorconsortium.org/
Professor of Biomolecular Engineering at the University of California, Santa Cruz; Associate Director, UC Santa Cruz Genomics Institute
Associate Professor of Biomolecular Engineering at the University of California, Santa Cruz; Associate Director, UC Santa Cruz Genomics Institute
