Role of haplotype map in CrosscheckFingerprint when no ANCHOR_SNPs are defined #8924
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harrymatthews50
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I have the job of assessing a pipeline (not implemented by me) for correctness. It is for somatic variant calling with paired tumour-normal samples. As part of the pipeline CrosscheckFingerprint is run comparing the tumour to normal. It is given a custom haploytype map that has no entries in the ANCHOR_SNP columnI .e. the haplotype map is not actually defining any haplotypes. What does CrosscheckFingerprint do with this information in this case (if anything)?
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