Explore Workflows
View already parsed workflows here or click here to add your own
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exome alignment and somatic variant detection for cle purpose
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![]() Path: definitions/pipelines/cle_somatic_exome.cwl Branch/Commit ID: bcc6adaf15035f5ce6fc851e27b1173b0fd20c1c |
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ani_top_n
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![]() Path: task_types/tt_ani_top_n.cwl Branch/Commit ID: 54c5074587af001a44eccb4762a4cb25fa24cb3e |
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bam to trimmed fastqs and HISAT alignments
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq_and_hisat_alignments.cwl Branch/Commit ID: 25aa4788dd4efb1cc8ed6f609cb7803896e4d28d |
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sec-wf.cwl
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![]() Path: tests/wf/sec-wf.cwl Branch/Commit ID: f94719e862f86cc88600caf3628faba6c0d05042 |
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umi molecular alignment fastq workflow
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![]() Path: definitions/pipelines/umi_molecular_alignment.cwl Branch/Commit ID: 86fbeb95ef85111f3b4c6bc2bba8f06cef64e157 |
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THOR - differential peak calling of ChIP-seq signals with replicates
What is THOR? -------------- THOR is an HMM-based approach to detect and analyze differential peaks in two sets of ChIP-seq data from distinct biological conditions with replicates. THOR performs genomic signal processing, peak calling and p-value calculation in an integrated framework. For more information please refer to: ------------------------------------- Allhoff, M., Sere K., Freitas, J., Zenke, M., Costa, I.G. (2016), Differential Peak Calling of ChIP-seq Signals with Replicates with THOR, Nucleic Acids Research, epub gkw680. |
![]() Path: workflows/rgt-thor.cwl Branch/Commit ID: 3fc68366adb179927af5528c27b153abaf94494d |
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any-type-compat.cwl
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![]() Path: cwltool/schemas/v1.0/v1.0/any-type-compat.cwl Branch/Commit ID: 478c2ffc09fb189c4f36ccb82aad945b3db5f9b3 |
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Get Proteins
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![]() Path: wf_bacterial_prot_src.cwl Branch/Commit ID: 54c5074587af001a44eccb4762a4cb25fa24cb3e |
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Nested workflow example
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![]() Path: tests/wf/nested.cwl Branch/Commit ID: f94719e862f86cc88600caf3628faba6c0d05042 |
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BWA index pipeline
This workflow indexes the input reference FASTA with bwa, and generates faidx and dict file using samtools. This index sample can then be used as input into the germline variant calling workflow, or others that may include this workflow as an upstream source. ### __Inputs__ - FASTA file of the reference genome that will be indexed. ### __Outputs__ - Directory containing the original FASTA, faidx, dict, and bwa index files. - stdout log file (output in Overview tab as well) - stderr log file ### __Data Analysis Steps__ 1. cwl calls dockercontainer robertplayer/scidap-gatk4 to index reference FASTA with bwa, and generates faidx and dict files using samtools ### __References__ - Li, H., & Durbin, R. (2009). Fast and accurate short read alignment with Burrows–Wheeler transform. Bioinformatics, 25(14), 1754–1760. |
![]() Path: workflows/bwa-index.cwl Branch/Commit ID: 30031ca5e69cec603c4733681de54dc7bffa20a3 |