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

SplitNCigarReads output bai file

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    Anton Kovalsky

    Hi Tamar Lahav, thanks for your question!

    The BAI file is the index for the BAM that allows for querying different positions, so both are necessary when you want to subset your data. GATK tools that take a BAM input usually also require the BAI as an input. 

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