Jun 182014
 

fCNV

:: DESCRIPTION

fCNV is a probabilistic method for non-invasive analysis of de novo CNVs in fetal genome based on maternal plasma sequencing

::DEVELOPER

Computational Biology Lab at the University of Toronto

:: SCREENSHOTS

N/A

:: REQUIREMENTS

  • Linux/MacOsx/WIndows
  • Python

:: DOWNLOAD

 fCNV

:: MORE INFORMATION

Citation:

Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing.
Rampášek L, Arbabi A, Brudno M.
Bioinformatics. 2014 Jun 15;30(12):i212-i218. doi: 10.1093/bioinformatics/btu292.

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