Impact of Genomic Variation on Function (IGVF) Consortium Collection
The Impact of Genomic Variation on Function (IGVF) Consortium (Link opens in a new window) aims to understand how genomic variation affects genome function, which in turn impacts phenotype. The National Human Genome Research Institute (NHGRI) is funding this collaborative program that brings together teams of investigators who will use state-of-the-art experimental and computational approaches to model, predict, characterize and map genome function, how genome function shapes phenotype, and how these processes are affected by genomic variation. These joint efforts will produce a catalog of the impact of genomic variants on genome function and phenotypes.
Plasmids
The collection will grow as the IGVF community systematically perturbs the genome to assess the impact of genomic variation on genome function and phenotype and shares their plasmid tools through Addgene.
| ID | Plasmid | Description | Vector Type | PI | Publication |
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Additional Resources
- The IGVF Consortium (Link opens in a new window) is funded by the National Human Genome Research Institute (NHGRI) (Link opens in a new window).
- Find IGVF Consortium publications on bioRxiv (Link opens in a new window) or PubMed (Link opens in a new window).