Workflow: rnaseq-pt1.cwl

Fetched 2024-04-20 05:57:56 GMT

Star/HTSeq RNA Seq Pipeline

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Inputs

ID Type Title Doc
reads File[]

Sequences to be mapped (e.g. RNA-seq FASTQ files)

threads Integer

Number of threads

gff_file File

Genomic features in the GFF format

star_genome Directory

Genome directory containing STAR genome indices

ref_gene_model File

Reference gene model in bed format

align_out_prefix String

STAR output files name prefix

Steps

ID Runs Label Doc
qc
../tools/fastqc.cwl (CommandLineTool)
trim
../tools/trim_galore.cwl (CommandLineTool)
align
../tools/STAR.cwl (CommandLineTool)
index
../tools/samtools-index.cwl (CommandLineTool)

samtools-index.cwl is developed for CWL consortium

merge_index
../tools/merge-secondary-file.cwl (ExpressionTool)
quantification
../tools/htseq-count.cwl (CommandLineTool)
read_distribution
../tools/read_distribution.cwl (CommandLineTool)

Outputs

ID Type Label Doc
align_logs File[]

STAR alignment log files

qc_reports File[]

FastQC reports for input sequences

aligned_read File

STAR alignments in SAM format

trim_reports File[]

Trim Galore! summary reports

trimmed_reads File[]

Input reads trimmed by Trim Galore!

aligned_read_index File

BAM files indexed by samtools

quantification_report File

HTSeq feature counts report

read_distribution_report File

RSeQC read distribution report

Permalink: https://w3id.org/cwl/view/git/bbe24d8d7fde2e918583b96805909a2867b749d6/workflows/rnaseq-pt1.cwl