Explore Workflows
View already parsed workflows here or click here to add your own
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workflow.cwl
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Path: flow_dispatch/2other_species/workflow.cwl Branch/Commit ID: f7894707dd30a0edd199d3b67c4c8678f64c90b3 |
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workflow.cwl
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Path: flow_dispatch/2working_files/workflow.cwl Branch/Commit ID: f7894707dd30a0edd199d3b67c4c8678f64c90b3 |
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process VCF workflow
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Path: definitions/subworkflows/strelka_process_vcf.cwl Branch/Commit ID: 295e7b7f51727c0f2d6cc86ce817449b2e8dba3c |
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env-wf3.cwl
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Path: cwltool/schemas/v1.0/v1.0/env-wf3.cwl Branch/Commit ID: 7bfd77118cdc80dd7150115dd7a1a7ee6046f6fe |
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cluster_blastp_wnode and gpx_qdump combined
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Path: task_types/tt_cluster_and_qdump.cwl Branch/Commit ID: 5282690e0f634a5f83107ba878fe62cbbb347408 |
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gp_makeblastdb
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Path: progs/gp_makeblastdb.cwl Branch/Commit ID: 505b91e41741ccbcd5ebd2b6a09a3be604f9ece3 |
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gp_makeblastdb
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Path: progs/gp_makeblastdb.cwl Branch/Commit ID: 2801ce53744a085580a8de91cd007c45146b51e8 |
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EMG assembly for paired end Illumina
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Path: workflows/emg-assembly.cwl Branch/Commit ID: 316831663e84623eb0e3a260af252fef441924d4 |
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allele-alignreads-se-pe.cwl
Workflow maps FASTQ files from `fastq_files` input into reference genome `reference_star_indices_folder` and insilico generated `insilico_star_indices_folder` genome (concatenated genome for both `strain1` and `strain2` strains). For both genomes STAR is run with `outFilterMultimapNmax` parameter set to 1 to discard all of the multimapped reads. For insilico genome SAM file is generated. Then it's splitted into two SAM files based on strain names and then sorted by coordinates into the BAM format. For reference genome output BAM file from STAR slignment is also coordinate sorted. |
Path: subworkflows/allele-alignreads-se-pe.cwl Branch/Commit ID: bfa3843bcf36125ff258d6314f64b41336f06e6b |
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conflict-wf.cwl#collision
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Path: cwltool/schemas/v1.0/v1.0/conflict-wf.cwl Branch/Commit ID: e59538cd9899a88d7e31e0f259bc56734f604383 Packed ID: collision |
