AnVIL Consortia

AnVIL hosts data from the following programs and also allows users to submit their own data to the platform.

Current Consortia

CCDG

The Centers for Common Disease Genomics are a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to multiple common disease phenotypes.

CMG

The Centers for Mendelian Genomics is a multi-center collaboration aimed at identifying the genes responsible for Mendelian phenotypes by whole exome and whole genome sequencing

GTEx

The Genotype-Tissue Expression (GTEx) project is an ongoing effort to build a comprehensive public resource to study tissue-specific gene expression and regulation. Samples were collected from 54 non-diseased tissue sites across nearly 1000 individuals, primarily for molecular assays including WGS, WES, and RNA-Seq.

1000 G

The 1000 Genomes Project, launched in January 2008, is an international research effort to establish variation profiles across the human population. This open access data set continues to be a valuable resource to geneticists.

eMERGE

The Electronic and MEdical Records and Genomics project (eMERGE) is a national network organized and funded by the NHGRI that combines DNA biorepositories with electronic medical record (EMR) systems for large scale, high-throughput genetic research in support of implementing genomic medicine.

Planned Consortia

The following consortia are planned for data ingestion. Additional consortia are under consideration and will be listed as they are approved.

  • Covid19hg - The COVID-19 host genetics initiative
  • CSER - Clinical Sequencing Evidence-Generating Research
  • GTExv9 - Genotype-Tissue Expression Project
  • HPP - Human Pan Genome Reference Consortium
  • NIA - National Institute of Aging
  • NIMH - National Institute of Mental Health
  • UDN - Undiagnosed Disease Network
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