Open source non-invasive prenatal testing platform and its performance in a public health laboratory

被引：19

作者：

Johansen, Peter ^{[1
]}

Richter, Stine R. ^{[1
]}

Balslev-Harder, Marie ^{[1
]}

Miltoft, Caroline B. ^{[3
]}

Tabor, Ann ^{[3
]}

Duno, Morten ^{[2
]}

Kjaergaard, Susanne ^{[1
]}

机构：

[1] Rigshosp, Copenhagen Univ Hosp, Dept Clin Genet, Chromosome Lab, DK-2100 Copenhagen, Denmark

[2] Rigshosp, Copenhagen Univ Hosp, Dept Clin Genet, Mol Genet Lab, DK-2100 Copenhagen, Denmark

[3] Rigshosp, Copenhagen Univ Hosp, Dept Obstet, Ctr Fetal Med & Pregnancy, DK-2100 Copenhagen, Denmark

来源：

PRENATAL DIAGNOSIS | 2016年 / 36卷 / 06期

关键词：

FREE FETAL DNA; MATERNAL PLASMA; ANEUPLOIDIES; POPULATION; DIAGNOSIS; FRACTION; GENOME;

D O I：

10.1002/pd.4819

中图分类号：

Q3 [遗传学];

学科分类号：

071007 ; 090102 ;

摘要：

ObjectiveThe objective of this study was to introduce non-invasive prenatal testing (NIPT) for fetal autosomal trisomies and gender in a Danish public health setting, using semi-conductor sequencing and published open source scripts for analysis. MethodsPlasma-derived DNA from a total of 375 pregnant women (divided into three datasets) was whole-genome sequenced on the Ion Proton platform and analyzed using a pipeline based on WISECONDOR for fetal autosomal aneuploidy detection and SeqFF for fetal DNA fraction estimation. We furthermore validated a fetal sex determination analysis. ResultsThe pipeline correctly detected 27/27 trisomy 21, 4/4 trisomy 18, and 3/3 trisomy 13 fetuses. Neither false negatives nor false positives (chromosomes 13, 18, and 21) were observed in our validation dataset. Fetal sex was identified correctly in all but one triploid fetus (172/173). SeqFF showed a strong correlation (R-2=0.72) to Y-chromosomal content of the male fetus samples. DiscussionWe have implemented NIPT into Danish health care using published open source scripts for autosomal aneuploidy detection and fetal DNA fraction estimation showing excellent false negative and false positive rates. SeqFF provides a good estimation of fetal DNA fraction. This coupled with an analysis of fetal sex that provides a complete NIPT workflow, which may easily be adapted for implementation in other public health laboratories. (c) 2016 John Wiley & Sons, Ltd.

引用

页码：530 / 536

页数：7

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