Explore Workflows
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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: d93911fa135411fbab99513e4a672056b30490ce |
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Whole genome alignment and somatic variant detection
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Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 026bba9511561246ad65458f0f55c88cead26fbd |
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RNA-Seq alignment and transcript/gene abundance workflow
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Path: definitions/pipelines/rnaseq.cwl Branch/Commit ID: 5c4125344b1b9125ad04d7e768ecc99901570a7a |
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FASTQ to BQSR
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Path: definitions/subworkflows/fastq_to_bqsr.cwl Branch/Commit ID: 7b4b489474473c3d2d992a838b89632c2b97dc2c |
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alignment for nonhuman with qc
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Path: definitions/pipelines/alignment_wgs_nonhuman.cwl Branch/Commit ID: fbeea265295ae596d5a3ba563e766be0c4fc26e8 |
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bacterial_kmer
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Path: bacterial_kmer/wf_bacterial_kmer.cwl Branch/Commit ID: 4def84df33963fc9ac9d5c5f804b911d01a0d9ad |
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Create Genomic Collection for Bacterial Pipeline, ASN.1 input
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Path: genomic_source/wf_genomic_source_asn.cwl Branch/Commit ID: 4def84df33963fc9ac9d5c5f804b911d01a0d9ad |
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varscan somatic workflow
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Path: definitions/subworkflows/varscan.cwl Branch/Commit ID: f7ac3eff79128831c9f7a565d5b187882f39aa58 |
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Apply filters to VCF file
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Path: definitions/subworkflows/filter_vcf_mouse.cwl Branch/Commit ID: 6949082038c1ad36d6e9848b97a2537aef2d3805 |
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taxonomy_check_16S
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Path: task_types/tt_taxonomy_check_16S.cwl Branch/Commit ID: 13b411d94a568e52797ba936732dc65f1a91bd41 |
