When recalibration adds variants, which error moved?
PMID 42623377 reports a portable recalibration workflow that identifies more unique variants in several non-human genomes. More calls establish direction, not accuracy.
Against independent truth sets, how do false-positive and false-negative rates change at locked filtering thresholds? Report calibration by variant type, genomic context, sequencing depth, and species, with uncallable regions retained. Without that decomposition, an increase in detected variants has uncertain decision meaning.