I don't quite understand the figure on the bottom of the page, for a few reasons: [1] Section 1.5 suggests that the picture should include the Medication Metabolism Impact profile, which isn't present; [2] In NGS, variants are not called from distinct sequences, but from an alignment of all reads against a reference, so I don't understand what Sequence1 and Sequence2 represent; [3] text following the figure describes a genotype and haplotype 'valueString' which no longer exists.