The AnVIL project's featured workspaces demonstrate common genomic analysis pipelines deployed using data and tools available on AnVIL.
These analyses utilize unrestricted public data along with reproducible workflows, allowing researchers to clone and execute the workspaces as a learning exercise or for adapting to their own research.
AnVIL Hosts Release 1 of the Human Pangenome Reference Consortium Data
The AnVIL is proud to host release 1 from the Human Pangenome Reference Consortium (HPRC). The HPRC is an international effort focused on developing an inclusive collection of human reference genomes that represent human haplotype diversity and the tool ecosystem needed to fully utilize this resource.
Announcing Seqr Availability in AnVIL
The Broad Institute's Seqr is being launched today in production within AnVIL to provide a platform for genomic data analysis for rare diseases. The availability of Seqr will enable researchers to analyze and annotate their data with seqr in the AnVIL platform as well as collaborate with other investigators as they choose.
NHGRI AnVIL Cloud Platform Now Supports Free Export of GTEx Data
In support of the evolving nature of the NHGRI mission, we are pleased to announce that researchers are now able to download controlled access GTEx V8 to local compute infrastructure without incurring egress fees.
Modeling the computing requirements and costs for genomics analysis in the cloud
The 2021 Genome Informatics Meeting will cover topics including Microbial and Metagenomics; Sequencing Algorithms, Variant Discovery and Genome Assembly; Evolution, Complex Traits and Phylogenetics; Functional Genomics; Single Cell Genomics; and Epigenetics and Genome Structure.