to remove a peak from a copy number data set and define a genomic interval of interest around
the peak.
Tumor genomes often contain multiple DNA copy number alterations, e.g., amplifications
or deletions. The locus that harbors the most extreme alteration, k, as evidenced by the maximum
or minimum column mean, provides a point estimate for the location of an underlying driver gene.
Also, loci near k may be affected by the same underlying genomic event. The peeling procedure is
applied to "nullify" entries in X that contribute to the alteration at k, thus making it possible
to identify altered regions elsewhere in the genome. This function is called by
peelingOneIterate.