Difference between revisions of "FusionSeq"

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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=Identifies fusion transcripts from paired end RNA-Seq data.
 
|sw summary=Identifies fusion transcripts from paired end RNA-Seq data.
|bio domain=Fusion transcripts, RNA-Seq
+
|bio domain=Fusion transcripts, RNA-Seq, Gene Fusions, Fusion Transcripts
|bio method=Alignment Analysis, Gene Fusions, Fusion Transcripts
+
|bio method=Alignment Analysis,  
 
|bio tech=Platform independent
 
|bio tech=Platform independent
 
|created by=Andrea Sboner, Lukas Habegger
 
|created by=Andrea Sboner, Lukas Habegger

Revision as of 22:34, 20 May 2011

Application data

Created by Andrea Sboner, Lukas Habegger
Biological application domain(s) Fusion transcripts, RNA-Seq, Gene Fusions, Fusion Transcripts
Principal bioinformatics method(s) Alignment Analysis
Technology Platform independent
Created at Yale University
Maintained? Yes
Input format(s) MRF
Output format(s) GFR, BP
Programming language(s) C
Licence Creative Commons - Attribution; Non-commercial 2.5
Operating system(s)
  • nix

, MacOS

Summary: Identifies fusion transcripts from paired end RNA-Seq data.

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Description

FusionSeq is a modular computational framework that detects fusion transcripts from RNASeq data. It is composed by three main modules: 1) a fusion detection modules, which identifies the potential fusion transcript candidates; 2) a filtration cascade module, which removes artifacts generated by several sources of noise, such as mismapping, random pairing during sample preparation, etc.; 3) a junction-sequence identifier module, which detect the sequence of the junction. Each fusion candidate is also ranked according to several statistic to help prioritize the experimental validation.





Links


References

  1. . 2010. Genome Biology
  2. . 2011. Genome Research


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