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github.com/broadinstitute/long-read-pipelines/SRWholeGenome_Simplified

Authors: Jonn Smith;

github.com/broadinstitute/long-read-pipelines/SRWholeGenome_Simplified

Abstract

This workflow performs single-sample variant calling on Illumina reads from one or more flow cells containing replicates of the same sample. The workflow merges multiple samples into a single BAM prior to variant calling.

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