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

CreateSomaticPanelOfNormals (BETA) Follow

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    Alex van Vliet

    Hi! Is it recommended to use GenomicsDBImport for WES data? Should I provide an intervals file that is essentially the target .bed?

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