CoNIFER uses exome sequencing data to find copy number variants (CNVs) and genotype the copy-number of duplicated genes.

Features

  • Can integrate exomes from multiple capture experiments
  • SVD normalization eliminates systematic bias and noise

Project Samples

Project Activity

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Categories

Bio-Informatics

License

GNU General Public License version 3.0 (GPLv3)

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CoNIFER Web Site

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Additional Project Details

Intended Audience

Science/Research

User Interface

Command-line

Programming Language

Python

Related Categories

Python Bio-Informatics Software

Registered

2011-10-24