| Literature DB >> 25585704 |
Baran Bayindir1,2, Luc Dehaspe1, Nathalie Brison1, Paul Brady1, Simon Ardui1, Molka Kammoun1, Lars Van der Veken3, Klaske Lichtenbelt3, Kris Van den Bogaert1, Jeroen Van Houdt1, Hilde Peeters1, Hilde Van Esch1, Thomy de Ravel1, Eric Legius1, Koen Devriendt1, Joris R Vermeesch1.
Abstract
Noninvasive prenatal testing by massive parallel sequencing of maternal plasma DNA has rapidly been adopted as a mainstream method for detection of fetal trisomy 21, 18 and 13. Despite the relative high accuracy of current NIPT testing, a substantial number of false-positive and false-negative test results remain. Here, we present an analysis pipeline, which addresses some of the technical as well as the biologically derived causes of error. Most importantly, it differentiates high z-scores due to fetal trisomies from those due to local maternal CNVs causing false positives. This pipeline was retrospectively validated for trisomy 18 and 21 detection on 296 samples demonstrating a sensitivity and specificity of 100%, and applied prospectively to 1350 pregnant women in the clinical diagnostic setting with a result reported in 99.9% of cases. In addition, values indicative for trisomy were observed two times for chromosome 7 and once each for chromosomes 15 and 16, and once for a segmental trisomy 18. Two of the trisomies were confirmed to be mosaic, one of which contained a uniparental disomy cell line. As placental trisomies pose a risk for low-grade fetal mosaicism as well as uniparental disomy, genome-wide noninvasive aneuploidy detection is improving prenatal management.Entities:
Mesh:
Year: 2015 PMID: 25585704 PMCID: PMC4592078 DOI: 10.1038/ejhg.2014.282
Source DB: PubMed Journal: Eur J Hum Genet ISSN: 1018-4813 Impact factor: 4.246