AnVIL API Library
Interact with AnVIL data, analysis solutions, and workflows via a command line interface.
Gen3 is a cloud-based software platform for managing, analyzing, harmonizing, and sharing large datasets. Gen3 is an open source platform for developing data commons.
Access thousands of tools via an intuitive graphical user interface for processing batch analysis with Galaxy Workflows and interactive downstream visualizations.
Dockstore is an open platform used by the GA4GH for sharing Docker-based tools described with the Common Workflow Language (CWL), the Workflow Description Language (WDL), or Nextflow (NFL).
Interactive analysis with the python or R programming languages; the R environment includes a family of Bioconductor 3.10 packages.
Interactive analysis with your favorite R coding platform.
Terra is an analysis platform that allows users to access data, run analysis tools, and collaborate. Terra is powered by Google Cloud Platform, enabling the user to scale and manage billing of their own projects.
Batch processing of GATK and other workflows.
View our training guides for onboarding to the Terra analysis engine.
Learn how to request access to AnVIL's high-value, access controlled, genomic datasets.
Work with the AnVIL team to contribute your consortium's data to AnVIL.
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.
This is a fully reproducible example of Processing For Variant Discovery, HaplotypeCallerGVCF, and Joint Discovery workflows based on GATK Best Practices.
This workspace contains an example of the somatic copy number variation workflow, representing the Variant Discovery portion of the Somatic CNV Discovery pipeline.
The Optimus pipeline processes 3-prime single-cell transcriptome data from the 10X Genomics v2 (and v3) assay.
The inferCNV workflow compares RNA from tumor samples with corresponding “normal” samples to identify evidence for copy number variations in tumors.
This workspace serves as a basic tutorial for using Hail, a python-based package containing additional data types and methods for working with genomic data.
Release Road Map
AnVIL is continually integrating new high-value data sets, platform components and tools.