
Talkowski Lab
119 posts

Talkowski Lab
@TalkowskiLab
Understanding the consequences of genomic variation in human disease.



Day 2 at @AGBT Precision Health 2024 brings another group of incredible speakers including Kyle Farh from @illumina, @aaronquinlan from @UofUGenetics and @ontowonka from @CUSystem. See you there! #AGBTPH

Day 2 at @AGBT Precision Health 2024 brings another group of incredible speakers including Kyle Farh from @illumina, @aaronquinlan from @UofUGenetics and @ontowonka from @CUSystem. See you there! #AGBTPH


START ME UP! Co-Chairs @NHGRI_Director from @genome_gov and Mike Talkowski from @MassGeneralNews and @TalkowskiLab take the stage and kick off Day 1 at AGBT Precision Health 2024. #AGBTPH

As part of #gnomAD v4, in collaboration with the @TalkowskiLab, we have released 1,199,117 genome SVs and 66,903 rare exome CNVs. These data represent the first gnomAD SV dataset released native to the GRCh38 reference genome. (1/2)

The #gnomAD team is proud to announce the release of gnomAD v4! The v4 dataset includes 730,947 exomes & 76,215 genomes, which is ~5x larger than the v2 & v3 releases combined, & includes nearly 120K indivs of non-European genetic ancestry broad.io/gnomad_v4 #ASHG23 (1/11)












Today is Genetic Counselor Awareness Day and gnomAD would like to recognize all the genetic counselors around the world working in clinics, labs, research, education and beyond. A special thank you to all our GC users and team members! #genechat #GCAD2022



Genomic constraint metric is now available on the #gnomAD browser. To learn more about the genomic constraint metric view the preprint on bioRxiv (biorxiv.org/content/10.110…) or attend @sc2643’s #ASHG22 platform presentation on 10/28 10:30am in rm 502


Super proud of Lily on a great ASHG talk!!! Handling all these questions like a champion. #ASHG22

