Workflow: RNA-Seq alignment and transcript/gene abundance workflow - first-stranded data

Fetched 2023-01-12 02:59:46 GMT
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Inputs

ID Type Title Doc
firststrand Boolean (Optional)
sample_name String
secondstrand Boolean (Optional)
read_group_id String[]
kallisto_index File
reference_index File
read_group_fields fc5165fa8f27e57c88e71d6985bd175c[]
trimming_adapters File
instrument_data_bams File[]
reference_annotation File
trimming_max_uncalled Integer
trimming_min_readlength Integer
trimming_adapter_trim_end String
gene_transcript_lookup_table File
trimming_adapter_min_overlap Integer

Steps

ID Runs Label Doc
merge
merge.cwl (CommandLineTool)
Sambamba: merge
kallisto
kallisto.cwl (CommandLineTool)
Kallisto: Quant
index_bam
../detect_variants/index_bam.cwl (CommandLineTool)
samtools index
stringtie
stringtie.cwl (CommandLineTool)
StringTie
transcript_to_gene
transcript_to_gene.cwl (CommandLineTool)
Kallisto: TranscriptToGene
bam_to_trimmed_fastq_and_hisat_alignments bam to trimmed fastqs and HISAT alignments

Outputs

ID Type Label Doc
final_bam File
gene_abundance File
transcript_abundance_h5 File
stringtie_transcript_gtf File
transcript_abundance_tsv File
stringtie_gene_expression_tsv File
Permalink: https://w3id.org/cwl/view/git/8f21f80a504c7fb834af331715a0661707d25537/rnaseq/workflow.cwl