1,009
edits
Changes
m
== Description ==
<!-- Describe the application in the space below -->
<!-- -->
Text replace - "Personal genomics" to "Personalised medicine"
{{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.
|bio domain=Genomics, Personal genomicsPersonalised medicine, Copy number estimation,
|bio method=Read depth analysis
|bio tech=Illumina/Solexa, Illumina,
|created by=Can Alkan
|created at=University of Washington
|output format=BED (copy numbers)
|language=C
|licence=Free for academicCommercial, Freeware, |os=All POSIX (Linux/BSD/UNIX-like OSes),
}}
{{Links}}
{{References}}
{{Link box}}