Workflow: RNA-Seq alignment with qc

Fetched 2023-01-04 08:30:25 GMT
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Inputs

ID Type Title Doc
fastq1 File
fastq2 File (Optional)
refgene File
genomeDir Directory
paired_end Boolean
rsem_reference String
annotation_file File
input_sort_order String

Steps

ID Runs Label Doc
fc
../tools/subread_featurecounts.cwl (CommandLineTool)
run subread v1.6.4
rsem
../tools/rsem.cwl (CommandLineTool)
run rsem v1.3.0
star
../tools/star.cwl (CommandLineTool)
run STAR v2.5.4
rseqc
../tools/rseqc.cwl (CommandLineTool)
run RSeQC v3.0.1
fastqc
../tools/fastqc.cwl (CommandLineTool)
run fastqc v0.11.8
preseq
../tools/preseq.cwl (CommandLineTool)
run preseq v2.0.3
sub_bam
../tools/sub_bam.cwl (CommandLineTool)
run summary
cutadapt
../tools/cutadapt.cwl (CommandLineTool)
run cutadapt v2.6
mark_dup
../tools/mark_duplicates_and_sort.cwl (CommandLineTool)
Mark duplicates and Sort
index_bam
../tools/index_bam.cwl (CommandLineTool)
samtools index
rnaseq_summary
../tools/rnaseqv4_summary.cwl (CommandLineTool)
run summary

Outputs

ID Type Label Doc
summary File[]
htmlfile File[]
final_bam File
genes_file File
zippedfile File[]
fastqc_data File[]
isoforms_file File
preseq_result File
transcript_file File
unique_stranded File
cutadapt_summary File
transcriptome_bam File
Permalink: https://w3id.org/cwl/view/git/0d4e517d7c1c6deb0db02d3746c8ed4db841bd57/definitions/pipelines/rnaseq4.cwl