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

How do I get the output of --bam-out from an exsiting vcf with HaplotypeCaller

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    Gökalp Çelik

    Hi shimijuan

    --bam-out must be activated during the time when variant calling is done therefore you cannot go back from a VCF to assembled haplotypes. Unfortunately you need to run HaplotypeCaller again for those regions that you have a variant of interest. 

    I hope this helps. 

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