genomeCoverageBed computes a histogram of feature coverage (e.g., aligned sequences) for a given genome. Optionally, by using the -d option, it will report the depth of coverage at each base on each chromosome in the genome file (-g).
Parent program: BEDTools
bedtools utilities are a swiss-army knife of tools for a wide-range of genomics analysis tasks. The most widely-used tools enable genome arithmetic: that is, set theory on the genome. For example, bedtools allows one to intersect, merge, count, complement, and shuffle genomic intervals from multiple files in widely-used genomic file formats such as BAM, BED, GFF, GTF, VCF. While each individual tool is designed to do a relatively simple task (e.g., intersect two interval files), quite sophisticated analyses can be conducted by combining multiple bedtools operations on the UNIX command line.