Explore Workflows
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qiime2 explore sample taxonomic composition
Taxonomic analysis from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
![]() Path: packed/qiime2-step2-dada2.cwl Branch/Commit ID: ef08cb00bd55b4c712645d171dbc691e01ed6165 Packed ID: qiime2-08-taxonomic-analysis.cwl |
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qiime2 DADA2 detect/correct sequence data
Option 1: DADA2 from https://docs.qiime2.org/2018.4/tutorials/moving-pictures/ |
![]() Path: packed/qiime2-step2-dada2.cwl Branch/Commit ID: ef08cb00bd55b4c712645d171dbc691e01ed6165 Packed ID: qiime2-03-dada2.cwl |
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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: be465ad19b07378f3f863f2c4e0019b420c859f2 |
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Filter single sample sv vcf from depth callers(cnvkit/cnvnator)
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![]() Path: definitions/subworkflows/sv_depth_caller_filter.cwl Branch/Commit ID: 3a822294da63b4e19446a285e2fef075e23cf3d0 |
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GSEApy - Gene Set Enrichment Analysis in Python
GSEAPY: Gene Set Enrichment Analysis in Python ============================================== Gene Set Enrichment Analysis is a computational method that determines whether an a priori defined set of genes shows statistically significant, concordant differences between two biological states (e.g. phenotypes). GSEA requires as input an expression dataset, which contains expression profiles for multiple samples. While the software supports multiple input file formats for these datasets, the tab-delimited GCT format is the most common. The first column of the GCT file contains feature identifiers (gene ids or symbols in the case of data derived from RNA-Seq experiments). The second column contains a description of the feature; this column is ignored by GSEA and may be filled with “NA”s. Subsequent columns contain the expression values for each feature, with one sample's expression value per column. It is important to note that there are no hard and fast rules regarding how a GCT file's expression values are derived. The important point is that they are comparable to one another across features within a sample and comparable to one another across samples. Tools such as DESeq2 can be made to produce properly normalized data (normalized counts) which are compatible with GSEA. |
![]() Path: workflows/gseapy.cwl Branch/Commit ID: 1f03ff02ef829bdb9d582825bcd4ca239e84ca2e |
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BAM to BEDPE
Comvert BAM to BEDPE and compress the output |
![]() Path: workflows/File-formats/bamtobedpe-gzip.cwl Branch/Commit ID: 00d21c7c7b35e4da3d272540f7356e9a63798442 |
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Subworkflow to allow calling different SV callers which require bam files as inputs
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![]() Path: definitions/subworkflows/single_sample_sv_callers.cwl Branch/Commit ID: e56f1024306aeb427d8aae2fff715ed2e8b8f86f |
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bam_readcount workflow
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![]() Path: definitions/subworkflows/bam_readcount.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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umi molecular alignment workflow
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![]() Path: definitions/subworkflows/molecular_alignment.cwl Branch/Commit ID: 35e6b3ef71b4a2a9caba1dbd5dc424a8809bcc0a |
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phase VCF
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![]() Path: definitions/subworkflows/phase_vcf.cwl Branch/Commit ID: e8b7759826df40b8bb821b40b15aea960a4951c4 |