GREGoR Consortium
@GREGoR_research
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Discovering causes of rare disease through innovative technology and vigorous collaboration. @NIH-funded. Tweets by Data Coordinating Center @UWBiostat.
USA
Joined October 2021
RT @HumanPangenome: A more complete understanding of human genetics starts with accurate, high-quality reference genomes. HPRC is building….
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RT @ClinGenResource: Excited to announce the ClinGen PGx Interpretation Committee's latest paper, “Towards an Integrated Resource for Pharm….
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RT @GeneticsSociety: Data sharing is crucial to advancing health research. The authors of @AJHGNews' latest article provide policy recommen….
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RT @useAnVIL: 🚨 Registration is OPEN for #AnVILCommunity2025 Conference! Join us in Nashville, Sept 3-5 for talks, posters, & CoFest!. - Re….
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RT @GA4GH: Join us for our next Fireside Chat this Friday, 11 July 2025 at 13:00 UTC, featuring a conversation with Tim Hubbard, Director o….
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RT @IGVFConsortium: Click editing is a recently developed platform that combines RNA-guided nickases and DNA-dependent polymerases to insta….
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RT @HumanPangenome: An emerging polishing pipeline, DeepPolisher, improves genome assemblies by reducing indel errors and correcting false….
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RT @IGVFConsortium: 🎉 Big milestone for our sister consortium, SMaHT!. Congrats on the paper in Nature, this is a huge step in mapping soma….
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RT @HGGAdvances: 📣New from Ng et al!.📄Identification of technically challenging variants – whole genome sequencing improves diagnostic yiel….
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RT @agbt: Great news! The abstract submission deadline for AGBT Precision Health is extended until July 14. You have extra time to contrib….
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RT @AJHGNews: 🫀New from Rai et al!.📄Genomic rare variant mechanisms for congenital cardiac laterality defect: A digenic model approach.http….
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RT @SMaHTnetwork: Coming soon in @Nature . The SMaHT marker paper officially goes live on July 3rd. From 19 tissue types and 150 donors,….
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RT @PNRIGenetics: Leadership news from PNRI: Jack Faris, PhD, is retiring as #CEO after helping guide the institute through a time of growt….
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RT @varianteffects: Do you know that we have a podcast series focused on the basic and translational science necessary to map the effect of….
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RT @varianteffects: In collaboration with Wellcome Connecting Science, we have a MAVE course coming up in November!.Multiplex assays of var….
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RT @IGVFConsortium: 🛠️ Topyfic is a Python library for applying reproducible LDA (rLDA) to single-cell and bulk RNA-seq data, helping ident….
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RT @HumanPangenome: Long- and short-read sequencing reveal four key telomere repeat changes shaping cancer genome evolution, offering a new….
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