Broad GDAC Firehose

Broad GDAC Firehose provides access to cancer genomics data across cohorts and data types, including RNA and methylation.

gdac.broadinstitute.org
Broad GDAC Firehose homepage screenshot

About Broad GDAC Firehose

Broad GDAC Firehose is a web-based platform hosted by the Broad Institute that provides access to aggregated cancer genomics datasets across dozens of disease cohorts. It supports multiple standardized data types per cohort, including RNA sequencing, methylation, copy number variation, mutation calls, and clinical data. Users can browse cohort-level data availability, with clear counts of cases and analyses listed for each cancer type. No raw data download functionality or integrated analysis tools are mentioned in available materials.

Key features

  • Access to cancer genomics data across dozens of disease cohorts
  • Supports multiple data types including RNA, methylation, and mutation calls
  • Displays case and analysis counts for each listed cancer cohort
  • Provides web-based browse access to cohort-level dataset metadata
Best for: Cancer genomics researchers seeking aggregated, cohort-level access to standardized cancer dataset metadata.
Good for
  • Aggregates cancer genomics data across a wide range of distinct disease cohorts
  • Includes multiple standardized data types per cohort to support comparative research
  • Provides clear case and analysis counts to help users assess dataset scale per cancer type
Watch out for
  • No raw data download functionality is indicated in available materials
  • Platform is proprietary, with no public source code or repository listed
  • No details on data licensing, update frequency, or curation standards are provided on the homepage

Broad GDAC Firehose at a glance

Type
Website
Pricing
Not confirmed. Check the site
Platforms
Web
Open source
Not stated
Last checked
Oct 6, 2026 · Online when checked
Listed
Oct 5, 2026

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Broad GDAC Firehose FAQ

What cancer genomics data types are available via the platform?
Available data types include RNA sequencing, methylation, copy number variation, mutation calls, and clinical data across cohorts.
Which cancer cohorts are included in the dataset collection?
Dozens of cancer types are represented, including breast, lung, colorectal, kidney, and brain cancers, with case and analysis counts listed per cohort.
Is raw dataset download available through the platform?
No download functionality is mentioned; only browse access to cohort-level data availability is provided.
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