Workflow Type: Galaxy
workflow-partial-bwa-mem
These workflows are part of a set designed to work for RAD-seq data on the Galaxy platform, using the tools from the Stacks program.
Galaxy Australia: https://usegalaxy.org.au/
Stacks: http://catchenlab.life.illinois.edu/stacks/
This workflow is part of the reference-guided stacks workflow, https://workflowhub.eu/workflows/347
Inputs
- demultiplexed reads in fastq format, may be output from the QC workflow. Files are in a collection.
- reference genome in fasta format
Outputs
- A set of filtered bam files, ready for the next part of the stacks workflow (e.g. gstacks).
- Statistics on the bam files.
Steps
ID | Name | Description |
---|---|---|
2 | BWA-MEM2 | toolshed.g2.bx.psu.edu/repos/iuc/bwa_mem2/bwa_mem2/2.2.1+galaxy0 |
3 | Samtools view: filters out unmapped and non-primary mapped reads (see flags) | toolshed.g2.bx.psu.edu/repos/iuc/samtools_view/samtools_view/1.13+galaxy2 |
4 | Samtools stats: BAM stats before filtering | toolshed.g2.bx.psu.edu/repos/devteam/samtools_stats/samtools_stats/2.0.3 |
5 | Samtools stats: BAM stats after filtering | toolshed.g2.bx.psu.edu/repos/devteam/samtools_stats/samtools_stats/2.0.3 |
6 | MultiQC: BAM stats before filtering | toolshed.g2.bx.psu.edu/repos/iuc/multiqc/multiqc/1.11+galaxy0 |
7 | MultiQC: BAM stats after filtering | toolshed.g2.bx.psu.edu/repos/iuc/multiqc/multiqc/1.11+galaxy0 |
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Created: 31st May 2022 at 09:05
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