Explore Workflows
View already parsed workflows here or click here to add your own
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Build STAR indices
Workflow runs [STAR](https://github.com/alexdobin/STAR) v2.5.3a (03/17/2017) PMID: [23104886](https://www.ncbi.nlm.nih.gov/pubmed/23104886) to build indices for reference genome provided in a single FASTA file as fasta_file input and GTF annotation file from annotation_gtf_file input. Generated indices are saved in a folder with the name that corresponds to the input genome. |
Path: workflows/star-index.cwl Branch/Commit ID: d1bef74924efcb8bfaa00987b3f148d5a192b7a9 |
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Genelists heatmap - peak and expression data visualized together
# Genelists heatmap - peak and expression data visualized together This visualization workflow takes as input 1 or more genelists derived from the DESeq and/or diffbind workflows along with user-selected samples and visualizes the ChIP/ATAC-Seq peak and/or RNA-Seq expression data visualized together in a single morpheus heatmap. ### __References__ - Morpheus, https://software.broadinstitute.org/morpheus |
Path: workflows/genelists-deseq-diffbind.cwl Branch/Commit ID: 549fac35bf6b8b1c25af0f4f6c3f162c40dc130e |
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blastp_wnode_struct
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Path: task_types/tt_blastp_wnode_struct.cwl Branch/Commit ID: 1e16653514fd5629a704516eb447043c9fd0a53b |
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Single-Cell Preprocessing Pipeline
Devel version of Single-Cell Preprocessing Pipeline =================================================== |
Path: workflows/single-cell-preprocess.cwl Branch/Commit ID: 954bb2f213d97dfef1cddaf9e830169a92ad0c6b |
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count-lines1-wf.cwl
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Path: tests/wf/count-lines1-wf.cwl Branch/Commit ID: 7bfe73a708dbf31d037303bb5a8fed1a79984b0f |
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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: 69623308d3b5577a4672b1d5aaf104ad1a259b20 |
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Trim Galore RNA-Seq pipeline single-read
The original [BioWardrobe's](https://biowardrobe.com) [PubMed ID:26248465](https://www.ncbi.nlm.nih.gov/pubmed/26248465) **RNA-Seq** basic analysis for a **single-end** experiment. A corresponded input [FASTQ](http://maq.sourceforge.net/fastq.shtml) file has to be provided. Current workflow should be used only with the single-end RNA-Seq data. It performs the following steps: 1. Trim adapters from input FASTQ file 2. Use STAR to align reads from input FASTQ file according to the predefined reference indices; generate unsorted BAM file and alignment statistics file 3. Use fastx_quality_stats to analyze input FASTQ file and generate quality statistics file 4. Use samtools sort to generate coordinate sorted BAM(+BAI) file pair from the unsorted BAM file obtained on the step 1 (after running STAR) 5. Generate BigWig file on the base of sorted BAM file 6. Map input FASTQ file to predefined rRNA reference indices using Bowtie to define the level of rRNA contamination; export resulted statistics to file 7. Calculate isoform expression level for the sorted BAM file and GTF/TAB annotation file using GEEP reads-counting utility; export results to file |
Path: workflows/trim-rnaseq-se.cwl Branch/Commit ID: dda6e8b5ada3f106a2b3bfcc1b151eccf9977726 |
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js_output_workflow.cwl
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Path: tests/wf/js_output_workflow.cwl Branch/Commit ID: 63f539ba60e91f0cb3ce7cda2c5da5c65525c375 |
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hmmsearch_wnode and gpx_qdump combined workflow to apply scatter/gather
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Path: task_types/tt_hmmsearch_wnode_plus_qdump.cwl Branch/Commit ID: 1ce371c7412debef75edf09e8830d74ac987a668 |
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mut3.cwl
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Path: tests/wf/mut3.cwl Branch/Commit ID: b82ce7ae901a54c7a062fd5eefd8d5ceb5a4d684 |
