nf-core/gatk4/haplotypecaller @ 0.0.0-6c4ed3a
Summary
Call germline SNPs and indels via local re-assembly of haplotypes
Get started
Add the following snippet to your workflow script to include this module.
include { GATK4_HAPLOTYPECALLER } from 'nf-core/gatk4/haplotypecaller'
License
MIT License
Name
|
GATK4_HAPLOTYPECALLER |
|---|
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}
|
intervals
file
|
Bed file with the genomic regions included in the library (optional) |
dragstr_model
file
|
Text file containing the DragSTR model of the used BAM/CRAM file (optional) *.txt
|
meta2
map
|
Groovy Map containing reference information e.g. [ id:'test_reference' ] |
|---|---|
fasta
file
|
The reference fasta file *.fasta
|
meta3
map
|
Groovy Map containing reference information e.g. [ id:'test_reference' ] |
|---|---|
fai
file
|
Index of reference fasta file fasta.fai
|
meta4
map
|
Groovy Map containing reference information e.g. [ id:'test_reference' ] |
|---|---|
dict
file
|
GATK sequence dictionary *.dict
|
meta5
map
|
Groovy Map containing dbsnp information e.g. [ id:'test_dbsnp' ] |
|---|---|
dbsnp
file
|
VCF file containing known sites (optional) |
meta6
map
|
Groovy Map containing dbsnp information e.g. [ id:'test_dbsnp' ] |
|---|---|
dbsnp_tbi
file
|
VCF index of dbsnp (optional) |
bam
tuple
meta
map
|
Groovy Map containing sample information e.g. [ id:'test', single_end:false ] |
|---|---|
*.realigned.bam
file
|
Assembled haplotypes and locally realigned reads *.realigned.bam
|
tbi
tuple
meta
map
|
Groovy Map containing sample information e.g. [ id:'test', single_end:false ] |
|---|---|
*.tbi
file
|
Index of VCF file *.vcf.gz.tbi
|
vcf
tuple
meta
map
|
Groovy Map containing sample information e.g. [ id:'test', single_end:false ] |
|---|---|
*.vcf.gz
file
|
Compressed VCF file *.vcf.gz
|
versions_gatk4
tuple
${task.process}
string
|
The name of the process |
|---|---|
gatk4
string
|
The name of the tool |
gatk --version | sed -n '/GATK.*v/s/.*v//p'
eval
|
The expression to obtain the version of the tool |
| Tool | Description | Homepage |
|---|---|---|
| gatk4 | Developed in the Data Sciences Platform at the Broad Institute, the toolkit offers a wide variety of tools with a primary focus on variant discovery and genotyping. Its powerful processing engine and high-performance computing features make it capable of taking on projects of any size. | https://gatk.broadinstitute.org/hc/en-us |
| Version | 0.0.0-6c4ed3a |
|---|