🚨 Excited to announce the Marker paper for the GREGoR Consortium! https://t.co/kP2zju1iRc
Accelerating #RareDisease diagnostics with cutting-edge #Genomics and global data sharing of omics and deep phenotyping from ~7500 individuals on NHGRI AnVIL and much more to come! 🧬
We are all walking mosaics of genetically distinct cells.
Every cell acquires around one mutation each division after fertilization, resulting in a vast amount of genetic diversity across all the cells in our bodies by the time we are born.
Join us TOMORROW for an inspiring #RareDiseaseDay2024#ScienceMatters seminar!
@fam177a1mamma shares her family's journey from undiagnosed children to research pioneers. @poseypod discusses @BCM-GREGoR rare disease research program. Register TODAY! https://t.co/4KeBCkeq3s
Thrilled to share I’m opening my lab @YaleGenetics in 2024! Excited to join the faculty of this amazing department. We’ll study human genetic variation in health & disease focusing on mitochondrial genomics
I’m #hiring, reach out if interested! #ASHG2023
https://t.co/i7aLFHAvVb
Heading to DC for #ASHG23?🧬
Register to join us for the @GREGoR_research Ancillary Session on Thursday 11/2 12:15 - 1:45pm ET featuring members @BenHeavner, Jen Posey (@poseypod), and Danny Miller (@danrdanny).
Registration:
https://t.co/N9B1747rfy
#ASHG2023@GeneticsSociety
@lizmizerik Can be a bit frustrating because not always obvious from the name whether it is a true ES/GS or some variation of that (eg only the coding genes).
🎆 Exciting research 🎆 @bcmhouston@bcmgenetics -- Dr. Ashok Balasubramanyam is researching why some diabetics don’t necessarily fit the box of type 1 and type 2 and what he’s discovered is there’s probably a wide range. 🧬 is key! https://t.co/8jq3e2AHHj
Pls RT: Places are filling up for our #Bioinformatics#Hackathon@BCM_HGSC (Aug 30-Sept 1). Come join us to work with us on new exciting projects across the 3 days (somatic variants, graph approach, RNA, SV etc).
@dnanexus#openscience@RiceCompSci
https://t.co/HWs6jj5xDw