News & Events
Meeting Free Weeks
Learn more about Heidi Rehm’s meeting free week campaign in Genomics and join the movement!
Read the gnomAD Papers
A collection of research articles from the gnomAD Consortium describing key analyses of the largest database of human genetic variation is out today in Nature, Nature Medicine, and Nature Communications.
The Broad Institute’s Response to COVID-19
Learn more about the Broad’s rapid response to the need for more COVID-19 testing in the midst of a pandemic.
-
Very excited to have this work out and a big thanks to @ksamocha and the rest of the gnomAD team for getting this o… https://t.co/hw567jgqRE -
RT @AnneOtation: Interested in classifying loss of function variants? We are looking for feedback on our advanced framework - check… https://t.co/fdm6dagKn3
-
RT @TheACMG: Participate! That’s the advice for #medstudents & trainees from ACMG Board of Directors Member Heidi Rehm, PhD, FAC… https://t.co/JGChqJaNBr
-
RT @gnomad_project: The #gnomAD browser now includes variant co-occurrence counts by gene. We hope this will help with interpretation o… https://t.co/mEX3fIjWJJ
-
Looking forward to #ACMGmtg23. Come join us at our ClinGen reception! RSVP info below. https://t.co/5T6iBCowll
-
RT @platzer_k: Downstream effect of uploads to #ClinVar: ⬆️ research opport. for all involved. We & @ZornitzaS talked about gettin… https://t.co/Izrckk68Wc
-
RT @ClinGenResource: NEW this week on ClinGen's website, https://t.co/1N3eq7MTty, Gene-Disease Validity Evidence Details. This new featu… https://t.co/ikwSnBbbwl
-
RT @GA4GH: The @PET_BioNews commissioned a survey to measure people’s understanding and attitudes towards areas of science and… https://t.co/tPdkCoD7OV
-
We are delighted to announce this year's call for applications supporting postdoctoral fellows for the NHGRI-funded… https://t.co/lcGSp7DFVK
-
We just published a commentary about the importance of adopting MANE transcripts (MANE Select as the default report… https://t.co/jNjxvgC49r