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Give two bam and one bed as input. Calculate the number of shared positions with more than xx depth. Calculate the number of identical positions with identical genotype with more than xx depth.
The text was updated successfully, but these errors were encountered:
Extracting snps-genotyped from the result after running snpahoy --minimum_coverage xx somatic ... gives the number of SNP positions with read depth xx in both samples.
The second part is a genuinely new feature. I will go ahead and implement that.
Give two bam and one bed as input. Calculate the number of shared positions with more than xx depth. Calculate the number of
identicalpositions with identical genotype with more than xx depth.The text was updated successfully, but these errors were encountered: