- Selected
- |
- Default Values
- Nested Workflows
- Tools
- Inputs/Outputs
This workflow is Open Source and may be reused according to the terms of:
MIT License
Note that the tools invoked by the workflow may have separate licenses.
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