| Literature DB >> 30501925 |
Meysam Rezaei1, Marnie Winter1, Deirdre Zander-Fox2, Clare Whitehead3, Jan Liebelt4, Majid Ebrahimi Warkiani5, Tristan Hardy6, Benjamin Thierry7.
Abstract
New tools for higher-resolution fetal genome analysis including microarray and next-generation sequencing have revolutionized prenatal screening. This article provides commentary on this rapidly advancing field and a future perspective emphasizing circulating fetal cell (CFC) utility. Despite the tremendous technological challenges associated with their reliable and cost-effective isolation from maternal blood, CFCs have a strong potential to bridge the gap between the diagnostic sensitivity of invasive procedures and the desirable noninvasive nature of cell-free fetal DNA (cffDNA). Considering the rapid advances in both rare cell isolation and low-input DNA analysis, we argue here that CFC-based noninvasive prenatal testing is poised to be implemented clinically in the near future.Keywords: circulating fetal cell; noninvasive prenatal testing; prenatal screening; rare cells
Mesh:
Substances:
Year: 2018 PMID: 30501925 DOI: 10.1016/j.tibtech.2018.11.001
Source DB: PubMed Journal: Trends Biotechnol ISSN: 0167-7799 Impact factor: 19.536