Explore Workflows
View already parsed workflows here or click here to add your own
Graph | Name | Retrieved From | View |
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Non-Coding Bacterial Genes
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![]() Path: bacterial_noncoding/wf_bacterial_noncoding.cwl Branch/Commit ID: 5463361069e263ad6455858e054c1337b1d9e752 |
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wf_clipseqcore_pe_2barcodes.cwl
Workflow for handling reads containing two barcodes. Returns the bam file containing read2 only. Notes: runs the following steps: - demultiplex - trimfirst_file2string - trimagain_file2string - b1_trim_and_map - view_r2 - index_r2_bam - make_bigwigs |
![]() Path: cwl/wf_clipseqcore_pe_2barcodes.cwl Branch/Commit ID: b4be31e4b809716f65354c0a3d0eff49949eabff |
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exome alignment with qc, no bqsr, no verify_bam_id
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![]() Path: definitions/pipelines/alignment_exome_mouse.cwl Branch/Commit ID: 06d2440d115b446c299b4ce96e8812d2f8df86ec |
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Seed Protein Alignments I
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![]() Path: protein_alignment/wf_seed_1.cwl Branch/Commit ID: 5463361069e263ad6455858e054c1337b1d9e752 |
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vecscreen.cwl
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![]() Path: vecscreen/vecscreen.cwl Branch/Commit ID: 1a6b9e5dea09caa0debbaff30ca39005dfa5e4d4 |
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scatter GATK HaplotypeCaller over intervals
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![]() Path: definitions/subworkflows/gatk_haplotypecaller_iterator.cwl Branch/Commit ID: 742dbafb5fb103d8578f48a0576c14dd8dae3b2a |
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STAR-Alignment-PE
This workflow aligns the fastq files using STAR for paired-end samples |
![]() Path: workflows/Alignments/star-alignment.cwl Branch/Commit ID: bab73c25f2358d9d76ffff13eeb39a5ece38a795 |
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vecscreen.cwl
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![]() Path: vecscreen/vecscreen.cwl Branch/Commit ID: a34f47d1e37af51e387ecdfa5c3047f106c1146b |
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rnaseq-alignment-quantification
This workflow retrieve SRA fastqc data and execute QC, alignment and quantification from TPMCalculator |
![]() Path: workflows/RNA-Seq/rnaseq-alignment-quantification.cwl Branch/Commit ID: bab73c25f2358d9d76ffff13eeb39a5ece38a795 |
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download_quality_control.cwl
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![]() Path: workflows/sra/download_quality_control.cwl Branch/Commit ID: bab73c25f2358d9d76ffff13eeb39a5ece38a795 |