Find genome variants and indels from RNA-seq (workflow)
From BioUML platform
Revision as of 12:21, 25 August 2015 by BioUML wiki Bot (Talk | contribs)
- 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
