Difference between revisions of "MrCaNaVaR"

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{{Bioinformatics application
 
{{Bioinformatics application
 
|sw summary=mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
 
|sw summary=mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.
|bio domain=Genomics, Personal genomics,
+
|bio domain=Genomics, Personal genomics, Copy number estimation,  
 
|bio method=Read depth analysis
 
|bio method=Read depth analysis
|bio tech=Illumina/Solexa, Illumina,  
+
|bio tech=Illumina,
 
|created by=Can Alkan
 
|created by=Can Alkan
 
|created at=University of Washington
 
|created at=University of Washington

Revision as of 04:37, 20 May 2011

Application data

Created by Can Alkan
Biological application domain(s) Genomics, Personal genomics, Copy number estimation
Principal bioinformatics method(s) Read depth analysis
Technology Illumina
Created at University of Washington
Maintained? Yes
Input format(s) SAM
Output format(s) BED (copy numbers)
Programming language(s) C
Licence Free for academic
Operating system(s) All POSIX (Linux/BSD/UNIX-like OSes)

Summary: mrCaNaVaR is a copy number caller that analyzes the next-generation sequence mapping read depth to discover large segmental duplications and deletions. It also has the capability of predicting absolute copy numbers of genomic intervals.

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