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



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    Pamela Bretscher

    Hi Oliver Ruebenacker,

    It looks like the "haplotype_database_b37 file that you're looking for is present on the "Workspace Data" tab of this workspace rather than within the b37Human reference data (see screenshot). I believe you will need to also import this file to your cloned workspace. Please let me know if this is helpful.

    Kind regards,


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