CNViewer 20111128 – Identification of Duplications, Insertions or LOH that Segregates with a Disease Phenotype

CNViewer 20111128

:: DESCRIPTION

CNViewer aids the identification of regions of abnormal copy number variation that segregates with a disease phenotype in small pedigree.

::DEVELOPER

Ian’s DNA@Leeds

:: SCREENSHOTS

CNViewer1

:: REQUIREMENTS

  • Windows
  • Microsoft .NET framework version 2.0 

:: DOWNLOAD

 CNViewer

:: MORE INFORMATION

Citation

PLoS One. 2012;7(8):e43466. doi: 10.1371/journal.pone.0043466. Epub 2012 Aug 17.
Rapid visualisation of microarray copy number data for the detection of structural variations linked to a disease phenotype.
Carr IM, Diggle CP, Khan K, Inglehearn C, McKibbin M, Bonthron DT, Markham AF, Anwar R, Dobbie A, Pena SD, Ali M.

CNViewer 2.1 – Analysis and Comparison of Copy Number Variation (CNV)

CNViewer 2.1

:: DESCRIPTION

CNViewer is a user-friendly tool for analysis and comparison of Copy Number Variation (CNV). It presents several functionalities such as add sensitive (usually clinical/phenotypic) data, export module, selection of genomic region of interest and supports three methods to input data.

::DEVELOPER

Cintia C. Palu

:: SCREENSHOTS

:: REQUIREMENTS

  • Web Browser

:: DOWNLOAD

 CNViewer

:: MORE INFORMATION