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

StrandBiasBySample Follow

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    Vee Koo

    Hi, I have created GVCFs with HaplotypeCaller ( and it seems that SB-values aren't showing if MIN_DP is present in the FORMAT field. Why is that?

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