This is a vector containing position (in base pair) of each variant site for the ReadCounts data in "Example.rda".  


This is a method for Allele-specific DNA Copy Number Profiling using Next-Generation Sequencing.  Given the allele-specific coverage at the variant loci, this program segments the genome into regions of homogeneous allele-specific copy number.  It requires, as input, the read counts for each variant allele in a pair of case and control samples. For detection of somatic mutations, the case and control samples can be the tumor and normal sample from the same individual.

pos: Position (bp)

Description

Arguments