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BCM Human Genome Sequencing Center

@bcmhgsc.bsky.social

A world leader in genomics, the Baylor College of Medicine Human Genome Sequencing Center advances biology & genetics through improved genome technologies.

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BCM Human Genome Sequencing Center@bcmhgsc.bsky.social · 4mo ago

Researchers Uncover Genetic Insights Into Human Diseases through ORIP's National Primate Research Centers. Great work from @bcmfromthelabs.bsky.social Drs. Jeffrey Rogers, Rui Chen, & Jun Wang. Read more: orip.nih.gov/about-orip/r...

Researchers Uncover Genetic Insights Into Human Diseases Through ORIP’s National Primate Research Centers | Office of Research Infrastructure Programs (ORIP) – DPCPSI – NIH

Nonhuman primates (NHPs) offer valuable insights into many diseases that affect human health because they are genetically and physiologically very similar to humans (Figure 1). ORIP’s National Primate...

orip.nih.gov

BCM Human Genome Sequencing Center@bcmhgsc.bsky.social · 5mo ago

Can AI reshape genomic discovery, clinical decision making, and patient-centered care? @theNASEM @bcmhouston.bsky.social #GenomicsRT #Genomics #GenomicsAI #HealthAI nationalacademies.org/units/HMD-HS...

Roundtable on Genomics and Precision Health

The Roundtable on Genomics and Precision Health brings together voices in the field to encourage innovation and actions that foster the wide adoption of and access to the benefits of genomics and prec...

nationalacademies.org

BCM Human Genome Sequencing Center@bcmhgsc.bsky.social · last yr.

Researchers supported by #TRISH at @bcmhouston.bsky.social develop the #GENESTAR manual, establishing guidelines for collecting omics data in space. Read here: blogs.bcm.edu/2025/06/10/s...

Invisible to the naked eye: Space omics and the need for sample collection guidelines - Baylor College of Medicine Blog Network

The GENESTAR manual establishes guidelines for collecting omics data in a spaceflight context, outlining TRISH’s Space Omics program.

blogs.bcm.edu

Moez Dawood@moezdawood.bsky.social · last yr.

🚨 Big news at #ACMG2025! 🚨 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)