Description

Map reads to contigs and estimate coverage

Input

name:type
description
pattern

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'sample1', single_end:false ]

input{:bash}

:file

FASTA/FASTQ containing reads (can be gzipped), or sorted BAM files of reads mapped to a reference. If supplying PE fasta for multiple samples, should be in the order “sample1_1, sample1_2, sample2_1, sample2_2…”.

*.{fa,fq,fa.gz,fq.gz,bam}

meta2{:bash}

:map

Groovy Map containing reference information e.g. [ id:'sample1', single_end:false ]

reference{:bash}

:file

Reference FASTA file to map reads to, or minimap2/strobealign index. Not required if using BAM input.

*.{fasta,fasta.gz,mmi,sti}

bam_input{:bash}

:boolean

True if input is bam files

interleaved{:bash}

:boolean

True if input is interleaved fastq file

Output

name:type
description
pattern

coverage{:bash}

meta{:bash}

:map

Groovy Map containing sample information e.g. [ id:'sample1', single_end:false ]

*.depths.{txt}

*.depth.txt{:bash}

:map

Groovy Map containing sample information e.g. [ id:'sample1', single_end:false ]

*.depths.{txt}

versions{:bash}

versions.yml{:bash}

:file

File containing software versions

versions.yml

Tools

coverm
GPL v3

CoverM aims to be a configurable, easy to use and fast DNA read coverage and relative abundance calculator focused on metagenomics applications