Workflow: RD_Connect

Fetched 2024-05-06 14:30:25 GMT
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Inputs

ID Type Title Doc
gqb Integer[]

Exclusive upper bounds for reference confidence GQ bands (must be in [1, 100] and specified in increasing order)

chromosome String

Label of the chromosome to be used for the analysis. By default all the chromosomes are used

fastq_files File[]

List of paired-end input FASTQ files

sample_name String

Sample name

readgroup_str String

Parsing header which should correlate to FASTQ files

known_sites_file File

VCF file correlated to reference genome assembly with know sites (for instance dbSNP)

reference_genome File[]

Compress FASTA files with the reference genome chromosomes

known_indels_file File

VCF file correlated to reference genome assembly with known indels

Steps

ID Runs Label Doc
gunzip
../tools/gunzip.cwl (CommandLineTool)
bwa_mem
../tools/bwa-mem.cwl (CommandLineTool)
bwa_index
../tools/bwa-index.cwl (CommandLineTool)
unzipped_known_sites
../tools/gunzip_known_sites.cwl (CommandLineTool)
unzipped_known_indels
../tools/gunzip_known_sites.cwl (CommandLineTool)

Outputs

ID Type Label Doc
gvcf File

unannotated gVCF output file from the mapping and variant calling pipeline

metrics File

Several metrics about the result

Permalink: https://w3id.org/cwl/view/git/31348ed533961f84cf348bf1af660ad9de6f870c/cwl-workflows/workflows/workflow.cwl