Runs of Homozygosity in WGS deep coverage.

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Francisco Ceballos

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Mar 24, 2017, 4:58:51 AM3/24/17
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I was wondering if its is possible to run --homozyg analisys using PLINK Seq, like in normal PLINK. Im looking to get runs of homozygosity from WGS deep coverage data but it seems that the current software does not support the amount of variants present. Thanks
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