Open joergi-w opened 3 years ago
We skip the base quality score recalibration for now.
Given the haplotype sequences. For each potential variant site: call genotypes and score them conditionally with respect to the haplotype likelihood.
GATK documentation
We skip the base quality score recalibration for now.
Given the haplotype sequences. For each potential variant site: call genotypes and score them conditionally with respect to the haplotype likelihood.
GATK documentation