Description

remove false positives of functional crispr genomics due to CNVs

Input

name:type
description
pattern

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

count_file{:bash}

:file

sgRNA raw counts

*.tsv

library_file{:bash}

:file

sgRNA library

*.tsv

min_reads{:bash}

:integer

Minimum number of reads

min_targeted_genes{:bash}

:integer

Minimum number of targeted genes

Output

name:type
description
pattern

norm_count_file{:bash}

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:‘test’, single_end:false ]

*_norm_table.tsv{:bash}

:file

normalized count file

*.tsv

versions{:bash}

versions.yml{:bash}

:file

File containing software versions

versions.yml