Meng Meng1, Xuchao Li2, Huijuan Ge2, Fang Chen3, Mingyu Han4, Yanyan Zhang2, Dongyang Kang4, Weiwei Xie2, Zhiying Gao4, Xiaoyu Pan2, Pu Dai4, Fanglu Chi5, Shengpei Chen2, Ping Liu2, Chunlei Zhang2, Jianjun Cao6, Hui Jiang3, Xun Xu7, Wei Wang8, Tao Duan1. 1. Shanghai First Maternity and Infant Hospital, Tongji University School of Medicine, Shanghai, China. 2. BGI-Shenzhen, Shenzhen, China. 3. 1] BGI-Shenzhen, Shenzhen, China [2] Department of Biology, University of Copenhagen, Copenhagen, Denmark. 4. Chinese PLA General Hospital, Beijing, China. 5. Eye, Ear, Nose and Throat Hospital, Fudan University, Shanghai, China. 6. 1] BGI-Shenzhen, Shenzhen, China [2] BGI-Shanghai, BGI-Shenzhen, Shenzhen, China. 7. 1] BGI-Shenzhen, Shenzhen, China [2] Shenzhen Birth Defect Screening Project Lab, BGI-Shenzhen, Shenzhen, China. 8. 1] BGI-Shenzhen, Shenzhen, China [2] Clinical Laboratory of BGI Health, Shenzhen, China.
Abstract
PURPOSE: The goals of our study were to develop a noninvasive prenatal test for autosomal recessive monogenic conditions and to prove its overall feasibility and potential for clinical integration. METHODS: We recruited a pregnant woman and her spouse, who had a proband child suffering from congenital deafness, and obtained the target-region sequencing data from a semicustom array that used genomic and maternal plasma DNA from three generations of this family. A haplotype-assisted strategy was developed to detect whether the fetus inherited the pathogenic mutations in the causative gene, GJB2. The parental haplotype was constructed using a trio strategy through two different processes, namely, the grandparent-assisted haplotype phasing process and the proband-assisted haplotype phasing process. The fetal haplotype was deduced afterward based on both the maternal plasma sequencing data and the parental haplotype. RESULTS: The accuracy levels of paternal and maternal haplotypes obtained by grandparent-assisted haplotype phasing were 99.01 and 97.36%, respectively, and the proband-assisted haplotype phasing process yielded slightly lower accuracies of 98.73 and 96.79%, respectively. Fetal inheritance of the pathogenic gene was deduced correctly in both processes. CONCLUSION: Our study indicates that the strategy of haplotype-based noninvasive prenatal testing for monogenic conditions has potential applications in clinical practice.
PURPOSE: The goals of our study were to develop a noninvasive prenatal test for autosomal recessive monogenic conditions and to prove its overall feasibility and potential for clinical integration. METHODS: We recruited a pregnant woman and her spouse, who had a proband child suffering from congenital deafness, and obtained the target-region sequencing data from a semicustom array that used genomic and maternal plasma DNA from three generations of this family. A haplotype-assisted strategy was developed to detect whether the fetus inherited the pathogenic mutations in the causative gene, GJB2. The parental haplotype was constructed using a trio strategy through two different processes, namely, the grandparent-assisted haplotype phasing process and the proband-assisted haplotype phasing process. The fetal haplotype was deduced afterward based on both the maternal plasma sequencing data and the parental haplotype. RESULTS: The accuracy levels of paternal and maternal haplotypes obtained by grandparent-assisted haplotype phasing were 99.01 and 97.36%, respectively, and the proband-assisted haplotype phasing process yielded slightly lower accuracies of 98.73 and 96.79%, respectively. Fetal inheritance of the pathogenic gene was deduced correctly in both processes. CONCLUSION: Our study indicates that the strategy of haplotype-based noninvasive prenatal testing for monogenic conditions has potential applications in clinical practice.