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  • oiiio
    Senior Member
    • Jan 2011
    • 105

    #1

    Using UnifiedGenotyper to call variants from haploid data?

    Has anyone tried to make indel calls from haploid data using UnifiedGenotyper?

    At the moment, I am not sure running the default parameters in this situation is the best practice. My first thought was to adjust the --heterozygosity and --indel_heterozygosity parameters to 0. However, this resulted in no calls being made whatsoever when I tried it with -glm INDEL.

    There is another thread with a similar question to this topic here:


    But, I would like to know about the GATK UnifiedGenotyper in particular for this haploid situation.

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