Explore Workflows
View already parsed workflows here or click here to add your own
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Cell Ranger Aggregate
Cell Ranger Aggregate ===================== |
![]() Path: workflows/cellranger-aggr.cwl Branch/Commit ID: 8049a781ac4aae579fbd3036fa0bf654532f15be |
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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: 8049a781ac4aae579fbd3036fa0bf654532f15be |
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workflow.cwl
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![]() Path: workflow/workflow.cwl Branch/Commit ID: 05f6f04fc3eef5bef3bd1d6b147c81040003340b |
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03-map-se.cwl
ATAC-seq 03 mapping - reads: SE |
![]() Path: v1.0/ATAC-seq_pipeline/03-map-se.cwl Branch/Commit ID: 1a0dd34d59ec983d1f7ad77bff35da2f016e3134 |
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pipeline-pe-blacklist-removal.cwl
ATAC-seq pipeline - reads: PE - with blacklist removal |
![]() Path: v1.0/ATAC-seq_pipeline/pipeline-pe-blacklist-removal.cwl Branch/Commit ID: 1a0dd34d59ec983d1f7ad77bff35da2f016e3134 |
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kmer_cache_store
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![]() Path: task_types/tt_kmer_cache_store.cwl Branch/Commit ID: 42df0c0f9a4e5697abadd9cb52440691fafc8f5d |
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Build Bismark indices
Copy fasta_file file to the folder and run run bismark_genome_preparation script to prepare indices for Bismark Methylation Analysis. Bowtie2 aligner is used by default. The name of the output indices folder is equal to the genome input. |
![]() Path: workflows/bismark-index.cwl Branch/Commit ID: 8049a781ac4aae579fbd3036fa0bf654532f15be |
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chipseq-gen-bigwig.cwl
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![]() Path: subworkflows/chipseq-gen-bigwig.cwl Branch/Commit ID: 3ceeb2e90f49579369b2e10485908516348381a9 |
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taxcheck.cwl
Perform taxonomic identification tasks on an input genome |
![]() Path: taxcheck.cwl Branch/Commit ID: e2a6cbcc36212433d8fbc804919442787a5e2a49 |
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Build Bowtie indices
Workflow runs [Bowtie](http://bowtie-bio.sourceforge.net/tutorial.shtml) v1.2.0 (12/30/2016) to build indices for reference genome provided in a single FASTA file as fasta_file input. Generated indices are saved in a folder with the name that corresponds to the input genome |
![]() Path: workflows/bowtie-index.cwl Branch/Commit ID: 8049a781ac4aae579fbd3036fa0bf654532f15be |