Abstract
Multiple-test procedures are increasingly important as technology increases
scientists’ ability to make large numbers of multiple measurements, as they do
in genome scans. Multiple-test procedures were originally defined to input a
vector of input p-values and an uncorrected critical p-value, interpreted as a
familywise error rate or a false discovery rate, and to output a corrected
critical p-value and a discovery set, defined as the subset of input p-values
that are at or below the corrected critical