Genome Analysis Toolkit

Variant Discovery in High-Throughput Sequencing Data

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Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. Learn more

Human genome reference builds - GRCh38 or hg38 - b37 - hg19 Follow

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    WangZiwei

    the Resource Bundle link points to a 404 NOT FOUND site

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