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, Copy number estimation,  
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|bio domain=Genomics, Personalised medicine, Copy number estimation,
 
|bio method=Read depth analysis
 
|bio method=Read depth analysis
 
|bio tech=Illumina,
 
|bio tech=Illumina,
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|output format=BED (copy numbers)
 
|output format=BED (copy numbers)
 
|language=C
 
|language=C
|licence=Free for academic
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|licence=Commercial, Freeware,
|os=All POSIX (Linux/BSD/UNIX-like OSes)
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|os=POSIX,
 
}}
 
}}
  

Latest revision as of 20:04, 19 December 2015

Application data

Created by Can Alkan
Biological application domain(s) Genomics, Personalised medicine, 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 Commercial, Freeware
Operating system(s) POSIX

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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