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Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing

The discovery of cell-free fetal DNA molecules in plasma of pregnant women has created a paradigm shift in noninvasive prenatal testing (NIPT). Circulating cell-free DNA in maternal plasma has been increasingly recognized as an important proxy to detect fetal abnormalities in a noninvasive manner. A...

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Autores principales: Peng, Xianlu Laura, Jiang, Peiyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343987/
https://www.ncbi.nlm.nih.gov/pubmed/28230760
http://dx.doi.org/10.3390/ijms18020453
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author Peng, Xianlu Laura
Jiang, Peiyong
author_facet Peng, Xianlu Laura
Jiang, Peiyong
author_sort Peng, Xianlu Laura
collection PubMed
description The discovery of cell-free fetal DNA molecules in plasma of pregnant women has created a paradigm shift in noninvasive prenatal testing (NIPT). Circulating cell-free DNA in maternal plasma has been increasingly recognized as an important proxy to detect fetal abnormalities in a noninvasive manner. A variety of approaches for NIPT using next-generation sequencing have been developed, which have been rapidly transforming clinical practices nowadays. In such approaches, the fetal DNA fraction is a pivotal parameter governing the overall performance and guaranteeing the proper clinical interpretation of testing results. In this review, we describe the current bioinformatics approaches developed for estimating the fetal DNA fraction and discuss their pros and cons.
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spelling pubmed-53439872017-03-16 Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing Peng, Xianlu Laura Jiang, Peiyong Int J Mol Sci Review The discovery of cell-free fetal DNA molecules in plasma of pregnant women has created a paradigm shift in noninvasive prenatal testing (NIPT). Circulating cell-free DNA in maternal plasma has been increasingly recognized as an important proxy to detect fetal abnormalities in a noninvasive manner. A variety of approaches for NIPT using next-generation sequencing have been developed, which have been rapidly transforming clinical practices nowadays. In such approaches, the fetal DNA fraction is a pivotal parameter governing the overall performance and guaranteeing the proper clinical interpretation of testing results. In this review, we describe the current bioinformatics approaches developed for estimating the fetal DNA fraction and discuss their pros and cons. MDPI 2017-02-20 /pmc/articles/PMC5343987/ /pubmed/28230760 http://dx.doi.org/10.3390/ijms18020453 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Peng, Xianlu Laura
Jiang, Peiyong
Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title_full Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title_fullStr Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title_full_unstemmed Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title_short Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
title_sort bioinformatics approaches for fetal dna fraction estimation in noninvasive prenatal testing
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5343987/
https://www.ncbi.nlm.nih.gov/pubmed/28230760
http://dx.doi.org/10.3390/ijms18020453
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