convert and then index CRAM -> BAM or 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
*.{bam,cram}
index
:file
BAM/CRAM index file
*.{bai,crai}
meta2
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
fasta
:file
Reference file to create the CRAM file
*.{fasta,fa}
fai
:file
Reference index file to create the CRAM file
*.{fai}
Output
name:type
description
pattern
bam
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
*.bam
:file
filtered/converted BAM file
*{.bam}
cram
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
*.cram
:file
filtered/converted CRAM file
*{cram}
bai
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
*.bai
:file
filtered/converted BAM index
*{.bai}
crai
meta
:map
Groovy Map containing sample information
e.g. [ id:‘test’, single_end:false ]
*.crai
:file
filtered/converted CRAM index
*{.crai}
versions_samtools
${task.process}
:string
The name of the process
samtools
:string
The name of the tool
samtools version | sed '1!d;s/.* //'
:eval
The expression to obtain the version of the tool
Topics
name:type
description
pattern
versions
${task.process}
:string
The name of the process
samtools
:string
The name of the tool
samtools version | sed '1!d;s/.* //'
:eval
The expression to obtain 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.
