Explore Workflows
View already parsed workflows here or click here to add your own
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Identifies non-coding RNAs using Rfams covariance models
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Path: workflows/cmsearch-multimodel-wf.cwl Branch/Commit ID: f3ffd2a753034c387b9a13a2932fb5c96f9ab029 |
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allele-vcf-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-vcf-alignreads-se-pe.cwl Branch/Commit ID: 6dca77dfd89996079bff84d07849a1583455b54f |
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sum-wf-noET.cwl
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Path: tests/sum-wf-noET.cwl Branch/Commit ID: 6397014050177074c9ccd0d771577f7fa9f728a3 |
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sec-wf.cwl
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Path: tests/wf/sec-wf.cwl Branch/Commit ID: baefdcb58fcc76e3378cf705fc6a3e69ef35bb47 |
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Nested workflow example
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Path: tests/wf/nested.cwl Branch/Commit ID: 7c7615c44b80f8e76e659433f8c7875603ae0b25 |
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io-int-wf.cwl
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Path: tests/io-int-wf.cwl Branch/Commit ID: 979083396fee912fca8ef778174216d317338a00 |
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dna.cwl#main
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Path: workflows/make-to-cwl/dna.cwl Branch/Commit ID: master Packed ID: main |
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io-int-default-wf.cwl
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Path: tests/io-int-default-wf.cwl Branch/Commit ID: ad91c844b5adfef514c059af364e20afc935e598 |
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mut.cwl
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Path: tests/wf/mut.cwl Branch/Commit ID: d5f7fa162611243f0c66dd3e933c16a4964a09ca |
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search.cwl#main
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Path: tests/search.cwl Branch/Commit ID: 3867f2fa4c204bc99dc664bb3f0ba71e360e142e Packed ID: main |
