Explore Workflows
View already parsed workflows here or click here to add your own
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_qc.cwl Branch/Commit ID: ec5355f335852e51c6938809c16ea1d230a3f983 |
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FastQC - a quality control tool for high throughput sequence data
FastQC - a quality control tool for high throughput sequence data ===================================== FastQC aims to provide a simple way to do some quality control checks on raw sequence data coming from high throughput sequencing pipelines. It provides a modular set of analyses which you can use to give a quick impression of whether your data has any problems of which you should be aware before doing any further analysis. The main functions of FastQC are: - Import of data from FastQ files (any variant) - Providing a quick overview to tell you in which areas there may be problems - Summary graphs and tables to quickly assess your data - Export of results to an HTML based permanent report - Offline operation to allow automated generation of reports without running the interactive application |
![]() Path: workflows/fastqc.cwl Branch/Commit ID: 7ced5a5259dbd8b3fc64456beaeffd44f4a24081 |
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Whole genome alignment and somatic variant detection
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![]() Path: definitions/pipelines/somatic_wgs.cwl Branch/Commit ID: 3bebaf9b70331de9f4845e2223c55082f5a812fb |
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heatmap-prepare.cwl
Workflow runs homer-make-tag-directory.cwl tool using scatter for the following inputs - bam_file - fragment_size - total_reads `dotproduct` is used as a `scatterMethod`, so one element will be taken from each array to construct each job: 1) bam_file[0] fragment_size[0] total_reads[0] 2) bam_file[1] fragment_size[1] total_reads[1] ... N) bam_file[N] fragment_size[N] total_reads[N] `bam_file`, `fragment_size` and `total_reads` arrays should have the identical order. |
![]() Path: tools/heatmap-prepare.cwl Branch/Commit ID: 46d3d403ddb240d5a8f4f31ab992b6d6a2686745 |
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bam to trimmed fastqs and biscuit alignments
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![]() Path: definitions/subworkflows/bam_to_trimmed_fastq_and_biscuit_alignments.cwl Branch/Commit ID: 51724b44c96e5fd849ae55b752865b80bc47d66c |
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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: a9133c999502acf94b433af8d39897e6c2cdf65f |
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Subworkflow that runs cnvkit in single sample mode and returns a vcf file
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![]() Path: definitions/subworkflows/cnvkit_single_sample.cwl Branch/Commit ID: ffab5424bb8b5905aecf6f8e2e6387da7f3df562 |
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mut3.cwl
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![]() Path: tests/wf/mut3.cwl Branch/Commit ID: e59538cd9899a88d7e31e0f259bc56734f604383 |
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cond-wf-011.cwl
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![]() Path: tests/conditionals/cond-wf-011.cwl Branch/Commit ID: a5073143db4155e05df8d2e7eb59d9e62acd65a5 |
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align_sort_sa
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![]() Path: task_types/tt_align_sort_sa.cwl Branch/Commit ID: be32f1363f9a9a9247d738e9593b207e9c5172c8 |