Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions-Reference-Cited by-同舟云学术

Non-invasive prenatal testing (NIPT) by low coverage genomic sequencing: Detection limits of screened chromosomal microdeletions

Published:2020-08-26 Issue:8 Volume:15 Page:e0238245
ISSN:1932-6203
Container-title:PLOS ONE
language:en
Short-container-title:PLoS ONE

Author:

Kucharik Marcel,Gnip Andrej,Hyblova Michaela,Budis Jaroslav,Strieskova Lucia,Harsanyova Maria,Pös Ondrej,Kubiritova Zuzana^ORCID,Radvanszky Jan,Minarik Gabriel,Szemes Tomas

Funder

the Operational Programme Research and Development funded by the European Research and Development Fund

Slovak Research and Development Agency

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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4. Accuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysis;S Taylor-Phillips;BMJ Open,2016

5. The accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis;FL Mackie;BJOG,2017

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