Today we’re announcing global democratization of deidentified allele count + frequency data with population breakdown from the first ~250k short-read WGS in All of Us designed to plug straight into clinical workflows. It is ~1.1 billion unique variants! 🧬💡
🧵 (1/4)
Today we’re announcing global democratization of deidentified allele count + frequency data with population breakdown from the first ~250k short-read WGS in All of Us designed to plug straight into clinical workflows. It is ~1.1 billion unique variants! 🧬💡
🧵 (1/4)
🗓 Friday, March 21, 1:30 PM PST
📍 Platform Session 8: Genomic Medicine and Education
🎙 Talk: GREGoR: Accelerating Genomics for Rare Diseases
🗓 Friday, March 21, 1:30 PM PST
📍 Platform Session 8: Genomic Medicine and Education
🎙 Talk: GREGoR: Accelerating Genomics for Rare Diseases
Join me at Booth 328 to learn about our technology, engage with our team, and grab some swag! Connect with our OhmX™ platform and the future of SV analysis.
Stop by to discuss how Nabsys can give your research a jolt with EGM #ACMG2025
We will be showcasing our upcoming rare disease products in our showcase, Advancing Rare Disease Diagnostics, on March 19th at 12:15 PM PST. Lunch will be provided. Register here: lnkd.in/gP847QVR
We will be showcasing our upcoming rare disease products in our showcase, Advancing Rare Disease Diagnostics, on March 19th at 12:15 PM PST. Lunch will be provided. Register here: lnkd.in/gP847QVR
Register for the meeting today! acmgmeeting.net
Register for the meeting today! acmgmeeting.net
📍Meet us at Booth 333 to learn how Constantiam Biosciences is advancing precision medicine with cutting-edge solutions for VUS resolution, rare disease diagnosis, and functional genomics.
#ACMGMtg25 #constantiambiosciences #ACMG2025
📍Meet us at Booth 333 to learn how Constantiam Biosciences is advancing precision medicine with cutting-edge solutions for VUS resolution, rare disease diagnosis, and functional genomics.
#ACMGMtg25 #constantiambiosciences #ACMG2025