Background
Noninvasive prenatal testing (NIPT) is one of the most commonly employed clinical measures for screening of fetal aneuploidy. Fetal Fraction (ff) has been demonstrated to be one of the key factors affecting the performance of NIPT. Accurate quantification of ff plays vital role in NIPT.
Methods
In this study, we present a new approach, the accurate Quantification of Fetal Fraction with Shallow‐Coverage sequencing of maternal plasma DNA (FF‐QuantSC), for the estimation of ff in NIPT. The method employs neural network model and utilizes differential genomic patterns between fetal and maternal genomes to quantify ff.
Results
Our results show that the predicted ff by FF‐QuantSC exhibit high correlation with the Y chromosome–based method on male pregnancies, and achieves the highest accuracy compared with other ff estimation approaches. We also demonstrate that the model generates statistically similar results on both male and female pregnancies.
Conclusion
FF‐QuantSC achieves high accuracy in ff quantification. The method is suitable for application in both male and female pregnancies. Since the method does not require additional information upon NIPT routines, it can be easily incorporated into current NIPT settings without causing extra costs. We believe that FF‐QuantSC shall provide valuable additions to NIPT.
A new flavonoid angelioue (1), and five known compounds, cuminatanol (2), myricetin (3), epigallocatechin (4), taxifolin (5) and dihydromyricetin (6), with good antibacterial and cytotoxic activities were isolated from the callus extract of Ampelopsis grossedentata.
In this research, a simple electrochemical sensor (c-MWCNTs/Nafion/GCE) was prepared by carboxylated multi-walled carbon nanotube, perfluorosulfonic acid polymer and glassy carbon electrode using drop coating method, and based on the obvious sensitization effect on the redox peak current of diethylstilbestrol (DES) in the presence of Co2+, a new electrochemical sensing method for the determination of DES in water was established. In a buffered solution of 0.2 mol l−1 NaH2PO4-Na2HPO4 at pH = 7.0, differential pulse voltammetry (DPV) was used when the Co2+ concentration was 20 μmol l−1. Under the optimized conditions of −0.2 ∼ −0.4 V (vs SCE), −0.2 V enrichment potential, and 120 s enrichment time, the concentration of DES showed a good linear relationship with the peak current over the range of 0.3 to 90 μmol l−1, and the detection limit(S/N = 3) was 0.01 μmol l−1. The actual water sample was detected, and the recovery was between 89.17% and 101.23%. This method had the characteristics of simple operation, low analysis cost and fast analysis speed, and had the potential application value of detecting DES in environmental water.
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