Allows one to find sequence variants and/or sites covered by a specified number of reads with bases above a set quality threshold. The tool works on six and ten column pileup formats produced with *samtools pileup* command. However, it also allows you to specify columns in the input file manually. |
hg clone https://toolshed.g2.bx.psu.edu/repos/devteam/pileup_parser
Name | Description | Version | Minimum Galaxy Version |
---|---|---|---|
on coverage and SNPs | 1.0.2 | any |