Migrate Your Genomic Research to the Cloud
Secure, cost-effective genomic analysis at scale.
Inverting the model of genomics data sharing with the NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL)AnVIL inverts the traditional model of genomic analysis, eliminating data movement and providing scalable, shared computing resources.
AnVIL Shorts: How can AnVIL help my research?Our short video series shows how AnVIL improves collaborative science for different researcher roles.
BioconductorAnalyze genomic data in the R statistical language.
GalaxyRun batch analysis workflows and interactive visualizations.
JupyterRun interactive analysis with python or R.
Access diverse, open and controlled access, cloud-hosted datasets
Create, share, and reuse reproducible analysis workspaces
Workspaces aggregate data and analysis methods. Start quickly from an existing workspace and customize it to your needs.Explore Workspaces
GATK - Best practices for somatic CNV discoveryA somatic copy number variation workflow, representing the Variant Discovery portion of the Somatic CNV Discovery pipeline.
GATK - Best Practices for Germline SNPs & IndelsA fully reproducible example of Processing For Variant Discovery, HaplotypeCallerGVCF, and Joint Discovery workflows.
Hail GWAS PIPELINEA basic tutorial for using Hail, a python-based package for working with genomic data.
inferCNV Tumor Single-Cell RNA-Seq Analysis PipelineCompare RNA from tumor samples with corresponding “normal” samples to identify evidence for copy number variations in tumors.