Description

Lofreq subcommand to call low frequency variants from alignments when tumor-normal paired samples are available

Input

Name
Description
Pattern

0 ()

1 ()

2 ()

3 ()

4 ()

5 ()

0 ()

1 ()

0 ()

1 ()

Output

Name
Description
Pattern

vcf ()

versions ()

Tools

lofreq Documentation

A fast and sensitive variant-caller for inferring SNVs and indels from next-generation sequencing data

doi: 10.1093/nar/gks918License: MIT
Authors