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mrCaNaVaR | Personalized copy number and segmental duplication maps using NGS

A copy number caller that analyzes the whole-genome next-generation sequence mapping read depth to discover large segmental duplications and deletions. mrCaNaVaR also has the capability of predicting absolute copy numbers of genomic intervals.

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mrCaNaVaR forum

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mrCaNaVaR classification

mrCaNaVaR specifications

Unique identifier:
OMICS_02138
Software type:
Package/Module
Restrictions to use:
Academic or non-commercial use
Biological technology:
Illumina
Programming languages:
C
Version:
0.51
Maintained:
Yes
Name:
micro-read Copy Number Variant Regions
Interface:
Command line interface
Input format:
SAM
Operating system:
Unix/Linux
Computer skills:
Advanced
Stability:
Stable

mrCaNaVaR distribution

versioning

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No versioning.

mrCaNaVaR support

Maintainer

  • Evan E. Eichler <>

Credits

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Publications

Institution(s)

Department of Genome Sciences, University of Washington School of Medicine, Seattle, WA, USA

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