Both methods, one target

Light theme

One specimen read twice — a capillary read and a deep amplicon run — on the same gene, in one session and one coordinate system. The column here is 252 reads deep and every one of them agrees; the row the readout names is the capillary read. Two methods answering the same question at the same position is the argument for keeping them together.

readhit with a Sanger read and NGS amplicon reads of the same specimen aligned to one reference gene in a single session, the Sanger row selected and the column reported as 252-fold deep, light theme
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