Produces comprehensive statistics from SAM/BAM/CRAM file
Input
name:type
description
pattern
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
input
:file
BAM/CRAM file from alignment
*.{bam,cram}
input_index
:file
BAI/CRAI file from alignment
*.{bai,crai}
meta2
:map
Groovy Map containing reference information
e.g. [ id:‘genome’ ]
fasta
:file
Reference file the CRAM was created with (optional)
*.{fasta,fa}
Output
name:type
description
pattern
stats
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
*.stats
:file
File containing samtools stats output
*.{stats}
versions_samtools
${task.process}
:string
Name of the process
samtools
:string
Name of the tool
samtools version | sed "1!d;s/.* //
:string
The command used to generate the version of the tool
Topics
name:type
description
pattern
versions
${task.process}
:string
The process the versions were collected from
samtools
:string
The tool name
samtools version | sed "1!d;s/.* //
:string
The command used to generate the version of the tool
Tools
samtools
MIT
SAMtools is a set of utilities for interacting with and post-processing
short DNA sequence read alignments in the SAM, BAM and CRAM formats, written by Heng Li.
These files are generated as output by short read aligners like BWA.