The AnVIL: Migrate Your Genomic Research To The Cloud

Có thể bạn quan tâm

Migrate Your Genomic Research to the Cloud

Secure, cost-effective genomic analysis at scale.

Learn MoreLaunch TerraAnVIL's cloudcompute environmentAnVIL November 2025 ReleaseExplore newly released and updated studies on the AnVIL platform - find datasets in the Data Explorer and Data Library.Learn More

GREGoR: accelerating genomics for rare diseasesThe GREGoR Consortium's latest publication in Nature (Vol 647) presents a large-scale collaborative framework, datasets and discoveries from over 7,500 individuals from over 3,000 families, are rapidly made available to researchers worldwide through the Analysis, Visualization and Informatics Lab-space (AnVIL) to catalyse global efforts to develop approaches for genetic diagnoses in rare diseasesPaperAmerican Society of Human Genetics Annual Meeting 2025The ASHG 2025 Annual Meeting will be held in Boston from October 14-18. The meeting will feature a wide range of scientific sessions, including plenary lectures, symposia, workshops, and poster presentations.Learn MoreIntroducing the All of Us + AnVIL Imputation ServiceThe Broad Institute's Data Sciences Platform has launched the All of Us + AnVIL Imputation Service.Learn MoreThe PRIMED Consortium: Reducing disparities in polygenic risk assessmentUsing the AnVIL, the PRIMED Consortium is developing methods to improve the performance of PRSs in global populations and individuals of diverse genetic ancestry.PaperA complete reference genome improves analysis of human genetic variationUsing the AnVIL, researchers find the T2T-CHM13 reference genome universally improves the analysis of human genetic variation.PaperWorkspaceInverting 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.PaperAnVIL Shorts: How can AnVIL help my research?Our short video series shows how AnVIL improves collaborative science for different researcher roles.Learn MorePhylogenetic analysis of SARS-CoV-2 in Boston highlights the impact of superspreading eventsUsing the AnVIL, researchers investigate the effect of superspreading events in the Boston area.PaperLearn MoreThe Dockstore: enhancing a community platform for sharing reproducible and accessible computational protocolsDockstore is an open source platform for publishing, sharing, and finding bioinformatics tools and workflows.PaperLearn MoreOrchestrating single-cell analysis with BioconductorThe AnVIL hosts a detailed book of single-cell methods and analysis techniques.PaperWorkspaceThe Galaxy platform for accessible, reproducible and collaborative biomedical analyses: 2020 updateAnVIL has access to full Galaxy capabilities, a computational workbench used by thousands of scientists to analyze biomedical data.PaperLearn More

Use your favorite platforms and tools

TerraCollaborate in Terra, AnVIL's secure, scalable, cloud compute environment.LaunchLearn More

BioconductorAnalyze genomic data in the R statistical language.Learn More Galaxy

GalaxyRun batch analysis workflows and interactive visualizations.Learn More

DockstoreCreate and share Docker-based workflows.LaunchLearn More

AnVIL Data ExplorerBuild cross study cohorts for analysis in Terra.DatasetsLearn More Jupyter

JupyterRun interactive analysis with python or R.Learn More Seqr

SeqrIdentify disease-causing variants.LaunchLearn More NCPI

NCPIInteroperate with other NIH data commons.Learn MoreDatasets

Explore

From curated tools and workflows to self-paced tutorials available on the Galaxy Training Network (GTN), there are plenty of materials to learn from.

Analysis Tools and WorkflowsCreate, reuse and share analysis and workflows in Jupyter, R Studio, and WDLDatasetsAccess public and managed-access data hosted in the AnVIL Data ExplorerExample WorkspacesExplore curated workspaces with popular datasets and analysesJoin our CommunityGet support at help.anvilproject.org

Access diverse, open and controlled access, cloud-hosted datasets

5PB+Size287k+Participants79Studies372Datasets

ALS-Compute

CARD

CCDG

Centers for Common Disease Genomics

CMG

Centers for Mendelian Genetics

CMH

Convergent Neuroscience

Convergent Neuro Consortium

CSER

Clinical Sequencing Evidence-Generating Research Consortium

eMERGE

Electronic and MEdical Records and Genomics Project

GREGoR

GTEx

The Genotype-Tissue Expression Project

HPRC

Human Pangenome Reference Consortium

PAGE

Population Architecture Using Genomics and Epidemiology

T2T

Telomere-to-Telomere

WGSPD1

1000G

The 1000 Genomes ProjectShow MoreConsortia RoadmapContribute Data

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

GATK - Best practices for somatic CNV discoveryA somatic copy number variation workflow, representing the Variant Discovery portion of the Somatic CNV Discovery pipeline. GATK

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. infer CNV

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.

Optimus PipelineThe Optimus pipeline processes 3-prime single-cell transcriptome data from the 10X Genomics v2 (and v3) assay.

Collaborate in a secure, cost-effective, scalable, cloud-based environment

Reduce compute and storage costs, reduce security and compliance overhead, scale to meet your needs.

Reduce Data Transfer Fees

There is no charge for data transferred from cloud storage to cloud compute within the same region.

Reduce Data Storage Costs

AnVIL hosted datasets are stored free of charge to researchers.

Collaborate Securely

Securely work with controlled-access data in Terra, AnVIL's FedRAMP Moderate compliant analysis platform.

Publish Reproducible Results

Share analyses and workspaces to demonstrate replicable and repeatable science.

Updates, training events, and workshops

Find out about AnVIL tool and platform updates, training opportunities, and conferences.

NewsEvents

Reporting Upcoming Changes to AnVIL Studies

Data corrections and consolidations effective the third week of January 2026.January 06, 2026

Do You Analyze NIH Data in a Compliant System? AnVIL Could Be Your Solution.

The NHGRI Genomic Data Science Analysis, Visualization, and Informatics Lab-space (AnVIL) has been formally recognized by the National Institutes of Health (NIH) as a Controlled-Access Data Repository (CADR).November 05, 2025

Complex Chromosomal Changes Involving Chromosome 9 Data Release on the AnVIL Platform

Sharing Our Data on AnVIL: Complex Chromosomal Changes Involving Chromosome 9.November 04, 2025Show All news

Recent Publications

Cite AnVILAdd Publication

Open-source Tools for Training Resources – OTTR

Candace Savonen, Carrie Wright, Ava M. Hoffman, John Muschelli, Katherine Cox, et al. (2022). Journal of Statistics and Data Science Education. https://doi.org/10.1080/26939169.2022.2118646.Show More

National Human Genome Research Institute Genomic Data Science Analysis, Visualization, and Informatics Lab-Space: Reaching out to Clinicians

Jennifer L. Hall, Sally Honeycutt, Nicole Gonzalez, Anne O'Donnell-Luria, Cassy Overby Taylor, et al. (2023). Circulation: Genomic and Precision Medicine. https://doi.org/10.1161/CIRCGEN.122.003936.Show More

Diversifying the genomic data science research community

The Genomic Data Science Community Network, et al. (2022). Genome Research. https://doi.org/10.1101/gr.276496.121.Show MoreShow all publications

Từ khóa » Nhgri