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

VariantAnnotator produces values different from those of HaplotypeCaller

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    Gökalp Çelik

    Hi Sofya Dubovskova

    VariantAnnotator does not use similar ways to analyze variant sites as HaplotypeCaller so numeric values could be different between 2 tools. VariantAnnotator uses direct reads to collect metrics however HaplotypeCaller has local assembly and realignment. 

    Regards. 

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    Sofya Dubovskova

    Thanks!

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