Oct 182013
 

CNIT 5.1

:: DESCRIPTION

CNIT is designed for Affymetrix GeneChip to analyze copy number of each SNP allele. CNIT can be applicable in chromosome-abnormal disease, cancer and copy number variation studies, and can provide accurate CN estimations with low false-positive rate.

::DEVELOPER

Cathy S.J. Fann lab,Institute of Biomedical Informatics, National Yang-Ming University, Taipei

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux / Windows
  • R package

:: DOWNLOAD

 CNIT

:: MORE INFORMATION

Citation

Genome-wide copy number analysis using copy number inferring tool (CNIT) and DNA pooling.
Lin CH, Huang MC, Li LH, Wu JY, Chen YT, Fann CS.
Hum Mutat. 2008 Aug;29(8):1055-62

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