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Description

This workflow pulls mapped read data from SNP-seek database and calls variants using the more recent and recommended HaplotypeCaller tool and best practices from GATK rather than the obsolete UnifiedGenotyper tool that was used to build the SNP-Seek database.

Requirements

  • Mapped reads for 2999 cultivars require around 15 TB of space
  • Variant calling requires Picard and GATK

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Workflow for calling variants using data from 3000 Rice Genomes project

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