A proof‐of‐concept study on the effects of low total cfDNA content and solutions to increase the NIPT trisomy 21 detection rate-Reference-Cited by-同舟云学术

A proof‐of‐concept study on the effects of low total cfDNA content and solutions to increase the NIPT trisomy 21 detection rate

Published:2019-09-30 Issue:2 Volume:34 Page:
ISSN:0887-8013
Container-title:Journal of Clinical Laboratory Analysis
language:en
Short-container-title:J Clin Lab Anal

Author:

Du Yang¹,Chen Ailing²,Yang Rui²,Zhou Tao²,Zhou Qin³,Yang Lan²,Wang Juan¹,Hong Yan¹,Chen Chen¹,Wan Qian¹,Yang Lin¹^ORCID,Chen Ying²

Affiliation:

1. Annoroad Gene Technology Co., Ltd Beijing China

2. Central Lab Wuxi Maternity and Child Health Care Hospital Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University Wuxi, Jiangsu China

3. Neonatal Department Wuxi Maternity and Child Health Care Hospital Affiliated Wuxi Maternity and Child Health Care Hospital of Nanjing Medical University Wuxi China

Funder

National Natural Science Foundation of China

Publisher

Wiley

Subject

Microbiology (medical),Biochemistry (medical),Medical Laboratory Technology,Clinical Biochemistry,Public Health, Environmental and Occupational Health,Hematology,Immunology and Allergy

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1002/jcla.23035

Reference19 articles.

1. Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis

2. Sequencing of Circulating Cell-free DNA during Pregnancy

3. Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics

4. Model-Based Analysis of Costs and Outcomes of Non-Invasive Prenatal Testing for Down’s Syndrome Using Cell Free Fetal DNA in the UK National Health Service

5. Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18

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2. Total number of reads affects the accuracy of fetal fraction estimates in NIPT;Molecular Genetics & Genomic Medicine;2021-03-09