Consequences of imprecision in fetal fraction estimation on performance of cell‐free DNA screening for Down syndrome
Author:
Affiliation:
1. Vanadis Diagnostics PerkinElmer Inc. Sollentuna Sweden
2. Faculty of Medicine Tel Aviv University Tel Aviv Israel
Publisher
Wiley
Subject
Genetics (clinical),Obstetrics and Gynecology
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/pd.6126
Reference30 articles.
1. Noninvasive prenatal screening for fetal aneuploidy, 2016 update: a position statement of the American College of Medical Genetics and Genomics
2. Position statement from the Chromosome Abnormality Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis
3. Screening for Fetal Chromosomal Abnormalities
4. Recommended practice for laboratory reporting of non-invasive prenatal testing of trisomies 13, 18 and 21: a consensus opinion
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1. Overview of Noninvasive Prenatal Testing (NIPT) for the Detection of Fetal Chromosome Abnormalities; Differences in Laboratory Methods and Scope of Testing;Clinical Obstetrics & Gynecology;2023-07-17
2. Association between low fetal fraction in cell‐free DNA screening and fetal chromosomal aberrations: A systematic review and meta‐analysis;Prenatal Diagnosis;2023-05-17
3. Position statement from the International Society for Prenatal Diagnosis on the use of non‐invasive prenatal testing for the detection of fetal chromosomal conditions in singleton pregnancies;Prenatal Diagnosis;2023-05-16
4. Screen‐positive rate in cell‐free DNA screening for microdeletion 22q11.2;Prenatal Diagnosis;2023-02-07
5. Variability in Fetal Fraction Estimation: Comparing Fetal Fractions Reported by Noninvasive Prenatal Testing Providers Globally;Clinical Chemistry;2022-12-28
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