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

CombineGVCFs Follow

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    yh guo

    Could I use CombineGVCFs to merge : [1] gvcf files produced from GenotypeGVCFs with --intervals different chrosomes and [2] some gvcf files produced from GenotypeGVCFs without --intervals argument to a single gvcf file?

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