fCNV
:: DESCRIPTION
fCNV is a probabilistic method for non-invasive analysis of de novo CNVs in fetal genome based on maternal plasma sequencing
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::DEVELOPER
Computational Biology Lab at the University of Toronto
:: SCREENSHOTS
N/A
:: REQUIREMENTS
- Linux/MacOsx/WIndows
- Python
:: DOWNLOAD
:: 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.