Description

This tools takes a background VCF, such as gnomad, that has full genome (though in some cases, users will instead want whole exome) coverage and uses that as an expectation of variants.

Input

Name
Description
Pattern

0 ()

1 ()

2 ()

0 ()

1 ()

2 ()

Output

Name
Description
Pattern

tsv ()

versions ()

Tools

htsnimtools Documentation

useful command-line tools written to show-case hts-nim

License: MIT
Authors