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Expert Rev Mol Diagn. 2015 Jan;15(1):111-24. doi: 10.1586/14737159.2015.973857. Epub 2014 Oct 27.

Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories.

Author information

1
Radboud University Medical Center, Nijmegen, Netherlands.

Abstract

Noninvasive prenatal testing (NIPT) for fetal aneuploidies using cell-free fetal DNA in maternal plasma has revolutionized the field of prenatal care and methods using massively parallel sequencing are now being implemented almost worldwide. Substantial progress has been made from initially testing for (an)euploidies of chromosomes 13, 18 and 21, to testing for sex chromosome (an)euploidies, additional autosomal aneuploidies as well as partial deletions and duplications genome-wide. Although NIPT is associated with significantly reduced risks for the fetus in comparison to existing invasive prenatal diagnostic methods, it presents several implementation challenges. Here, we review key issues potentially influencing NIPT and illustrate them using both data from literature and in-house data.

KEYWORDS:

NGS; NIPT; depth of coverage; noninvasive; prenatal; whole genome sequencing

PMID:
25347354
DOI:
10.1586/14737159.2015.973857
[Indexed for MEDLINE]

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