Просмотр кода страницы Normalized chromosome value

'''Normalized chromosome value''' (NCV) is a mathematical calculation for comparing each [[chromosome]] under tested in [[Cell-free fetal DNA|cell free DNA]] (cfDNA) for detecting genetic disorder of the fetus. NCV calculation removes variation within and between [[sequencing]] runs to optimize test precision.<ref>{{cite web|url=http://www.verinata.com/providers/clinical-data/ |title=Clinical Data |publisher=Verinata |date=2012-01-11 |access-date=2013-08-19}}</ref><ref>{{cite journal | title=Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood.  |vauthors=Sehnert AJ, etal | journal=Clin. Chem. |date=Jul 2011 | volume=57 | issue=7 | pages=1042–9 | doi=10.1373/clinchem.2011.165910|pmid=21519036 | doi-access=free }}</ref>

==References==
{{Reflist}}

[[Category:Genetics]]


{{genetics-stub}}