Difference between revisions of "Find genome variants and indels from RNA-seq (workflow)"
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Revision as of 12:21, 25 August 2015
- Workflow title
- Find genome variants and indels from RNA-seq
- Provider
- geneXplain GmbH
Workflow overview
Parameters
- Input fastq file
- Minimum read segment length
- We recommend set this value to about half the read length because TopHat will work better with multiple segments
- OutputFolder
- Results are here