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)

(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to: navigation, search
Workflow title
Find genome variants and indels from RNA-seq
Provider
geneXplain GmbH

Workflow overview

Find-genome-variants-and-indels-from-RNA-seq-workflow-overview.png

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
Personal tools
Namespaces

Variants
Actions
BioUML platform
Community
Modelling
Analysis & Workflows
Collaborative research
Development
Virtual biology
Wiki
Toolbox