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Analysis of the short fragments of fetal DNA enrichment to identify false positive cases of maternal origin in noninvasive prenatal testing |
1. Dongguan Maternal and Child Health Care Hospital,Dongguan,Guangdong Province,523107;2.School of basic medicine, Guangdong Medical University |
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Abstract To explore the clinical value of fetal DNA short fragment enrichment analysis for identifying false positive cases from maternal sources in noninvasive prenatal testing (NIPT). Methods:13 samples with NIPT false positive from maternal chromosomal abnormalities and 8 samples with NIPT false positive from placental chromosomal abnormalities were selected in this study. After sequencing by semi-conductor gene sequencing technology, the sequencing data were analyzed by fetal DNA full-fragment analysis (M method) and DNA short-fragment enrichment analysis (L method), respectively, to obtain the chromosome Z value and the corresponding chromosome position-dose distribution curve. Results: In maternal false-positive samples, the positive signal of L method was reduced compared with that of M method, which’s absolute value of Z value was decreased, and which’s line was closer to baseline 0 compared with M method on the chromosomal position-dose distribution curve. While the positive signal from the placenta sample was the opposite. Conclusion: In NIPT, DNA short fragment enrichment analysis can accurately identify the source of false positive signals from maternal sources without additional experimental costs, which has certain clinical application value.
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