posted on 2015-10-08, 03:42authored byMichael A. DeJesus, Chaitra Ambadipudi, Richard Baker, Christopher Sassetti, Thomas R. Ioerger
Reads in .fasta, .fastq or fastq.gz format are taken in as input, and mapped to the genome to get read-counts at individual TA sites. A .wig formatted file is returned as output, containing the coordinates and the read-counts at all TA sites in the genome.