Data from various genomics file formats (BAM, VCF, BED, etc), and sequencing technologies.

Sequencing data and analysis of 10 trios. First complete human genome assembly.

Reference data from several sequencing technologies. Used as ground truth for benchmarking.

Sequencing data from COVID-19 samples, processed through Illumina, PacBio and ONT.

Sequencing data and analysis of >2,500 individuals from around the world.

Sample data used for testing and benchmarking the DeepVariant variant caller.

Sample datasets from the Broad Institute for testing bioinformatics workflows.

Microbiome dataset of 300 healthy adults, and several individuals suffering from disease conditions.

Sequencing datasets and reference genomes of several threatened Australasian species.

Sequencing data and analysis of >3,000 rice varieties from 89 countries.

Test datasets for the GATK variant caller, with data from WGS, WES, and RNA-seq.