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CoNIFER

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Homepage for CoNIFER (Copy Number Inference From Exome Reads)

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Description

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

CoNIFER Web Site

Features

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

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Additional Project Details

Intended Audience

Science/Research

User Interface

Command-line

Programming Language

Python

Registered

2011-10-24
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