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

Fetched 2024-04-26 17:43:27 GMT
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Inputs

ID Type Title Doc
strand String
refFlat File
firststrand Boolean (Optional)
sample_name String
secondstrand Boolean (Optional)
read_group_id String[]
kallisto_index File
reference_index File
read_group_fields 24ec33a3b66b04e67ea5ad894535da2c[]
trimming_adapters File
ribosomal_intervals 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
generate_qc_metrics
generate_qc_metrics.cwl (CommandLineTool)
Picard: RNA Seq Metrics
bam_to_trimmed_fastq_and_hisat_alignments bam to trimmed fastqs and HISAT alignments

Outputs

ID Type Label Doc
chart File
metrics File
final_bam File
gene_abundance File
fusion_evidence 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/d1ee6a2a323cee7e4af00c7e0b926c2192038e1d/rnaseq/workflow.cwl