Next generation sequencing and the impact on prenatal diagnosis.

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Next generation sequencing and the impact on prenatal diagnosis.

Expert Rev Mol Diagn. 2018 Jul 02;:

Authors: Mellis R, Chandler N, Chitty LS

Abstract
INTRODUCTION: The advent of affordable and rapid next generation sequencing has been transformative for prenatal diagnosis. Sequencing of cell-free DNA in maternal plasma has enabled the development of not only a highly sensitive screening test for fetal aneuploidies, but now definitive non-invasive prenatal diagnosis for monogenic disorders at an early gestation. Sequencing of fetal exomes offers broad diagnostic capability for pregnancies with unexpected fetal anomalies, improving the yield and accuracy of diagnoses and allowing better counselling for parents. The challenge now is to translate these approaches into mainstream use in the clinic. Areas covered: Here, the authors review the current literature to describe the technologies available and how these have evolved. The opportunities and challenges at hand, including considerations for service delivery, counselling, and development of ethical guidelines, are discussed. Expert Commentary: As technology continues to advance, future developments may be towards non-invasive fetal whole exome or whole genome sequencing and a universal method for non-invasive prenatal diagnosis without the need to sequence both parents or an affected proband. Expansion of cell-free fetal DNA analysis to include the transcriptome and the methylome is likely to yield clinical benefits for monitoring other pregnancy-related pathologies such as pre-eclampsia and intrauterine growth restriction.

PMID: 29962246 [PubMed – as supplied by publisher]

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