CNIT

 
  • Full Name:Copy Number Inferring Tool
  • Description:Copy number inferring tool (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.
  • Authors:Cathy S. J. Fann
  • Operating Systems:Linux , MS-Windows
  • Supplementary data for the application of CNIT in gene expression analysis
Supplementary Table 1A.xls Supplementary Table 1B.xls Supplementary Table 1C.xls
Supplementary Table 2A.xls Supplementary Table 2B.xls Supplementary Table 2C.xls
Supplementary Table 3A.xls Supplementary Table 3B.xls
 

 

Download

Operating System Reference group Update Version Download
Windows 200 multi-ethnic unrelated individuals 2008/1/1 VW1.1 Chick here
UNIX 200 multi-ethnic unrelated individuals 2008/1/1 VU1.1 Chick here
Windows 210 HapMap unrelated individuals 2008/4/1 VW1.2 Chick here
UNIX 210 HapMap unrelated individuals 2008/4/1 VU1.2 Chick here
Windows 210 HapMap unrelated individuals 2008/6/1 VW5.1 Chick here
UNIX 210 HapMap unrelated individuals 2008/6/1 VU5.1 Chick here

 

* If you have any question or suggestion, please contact us at (csjfann@ibms.sinica.edu.tw).

* This software comes free for non-commercial use, and with no warranty whatsoever.

 

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