Cargando…

Response to “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”

Detalles Bibliográficos
Autores principales:	Muzzey, Dale, Haverty, Carrie, Evans, Eric A., Goldberg, James D.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2017
Materias:	Correspondence
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5811916/ https://www.ncbi.nlm.nih.gov/pubmed/28675624 http://dx.doi.org/10.1002/pd.5071

Ejemplares similares

Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk
por: Muzzey, Dale, et al.
Publicado: (2019)

Comment on “Noninvasive prenatal screening at low fetal fraction: comparing whole‐genome sequencing and single‐nucleotide polymorphism methods”
por: Ryan, Allison, et al.
Publicado: (2017)

Inaccuracies and shortcomings in “Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations”
por: Johansen Taber, Katherine, et al.
Publicado: (2019)

The impact of HBB‐related hemoglobinopathies carrier status on fetal fraction in noninvasive prenatal screening
por: Putra, Manesha, et al.
Publicado: (2022)

Technology-Driven Noninvasive Prenatal Screening Results Disclosure and Management
por: Arjunan, Aishwarya, et al.
Publicado: (2020)

High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening
por: Welker, Noah C., et al.
Publicado: (2020)

Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens
por: Kaseniit, Kristjan Eerik, et al.
Publicado: (2018)

Clinical experience across the fetal‐fraction spectrum of a non‐invasive prenatal screening approach with low test‐failure rate
por: Hancock, S., et al.
Publicado: (2020)

Cell‐free DNA fetal fraction in twin gestations in single‐nucleotide polymorphism‐based noninvasive prenatal screening
por: Hedriana, Herman, et al.
Publicado: (2019)

Correction: Inaccuracies and shortcomings in “Adherence of cell-free DNA noninvasive prenatal screens to ACMG recommendations”
por: Taber, Katherine Johansen, et al.
Publicado: (2019)

Factors Affecting the Fetal Fraction in Noninvasive Prenatal Screening: A Review
por: Deng, Cechuan, et al.
Publicado: (2022)

Reply
por: Hancock, S., et al.
Publicado: (2020)

Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening
por: Dang, Minghao, et al.
Publicado: (2019)

Correction: Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening
por: Dang, Minghao, et al.
Publicado: (2019)

Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing
por: Peng, Xianlu Laura, et al.
Publicado: (2017)

Re: Clinical experience across the fetal‐fraction spectrum of a non‐invasive prenatal screening approach with low test‐failure rate
por: Jelsema, R., et al.
Publicado: (2020)

White blood cell count affects fetal fraction and test failure rates in noninvasive prenatal screening
por: Qiao, Longwei, et al.
Publicado: (2023)

False Low-Risk Single Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in Pentasomy 49,XXXXY
por: Putra, Manesha, et al.
Publicado: (2018)

Maternal and fetal factors influencing fetal fraction: A retrospective analysis of 153,306 pregnant women undergoing noninvasive prenatal screening
por: Deng, Cechuan, et al.
Publicado: (2023)

Noninvasive Prenatal Measurement of the Fetal Genome
por: Fan, H. Christina, et al.
Publicado: (2012)

Noninvasive fetal genotyping of single nucleotide variants and linkage analysis for prenatal diagnosis of monogenic disorders
por: Wu, Wenman, et al.
Publicado: (2022)

Comment on “Commercial landscape of noninvasive prenatal testing in the United States”
por: Rabinowitz, Matthew
Publicado: (2013)

Calculating the fetal fraction for noninvasive prenatal testing based on genome‐wide nucleosome profiles
por: Straver, Roy, et al.
Publicado: (2016)

Hemolysis and Fetal Fraction in Cell-Free DNA Blood Collection Tubes for Noninvasive Prenatal Testing
por: Stokowski, Renee, et al.
Publicado: (2020)

A multivariate modeling method for the prediction of low fetal fraction before noninvasive prenatal testing
por: Hu, Liang, et al.
Publicado: (2021)

Noninvasive prenatal testing for fetal subchromosomal copy number variations and chromosomal aneuploidy by low‐pass whole‐genome sequencing
por: Yu, Dongyi, et al.
Publicado: (2019)

Combined fetal fraction to analyze the Z-score accuracy of noninvasive prenatal testing for fetal trisomies 13, 18, and 21
por: Yang, Jiexia, et al.
Publicado: (2023)

Combining the use of a fetal fraction‐based risk algorithm and probability of an informative redraw in noninvasive prenatal testing for fetal aneuploidy
por: Benn, Peter, et al.
Publicado: (2019)

Noninvasive prenatal screening for fetal common sex chromosome aneuploidies from maternal blood
por: Zhang, Bin, et al.
Publicado: (2017)

Evaluation of a Microhaplotype-Based Noninvasive Prenatal Test in Twin Gestations: Determination of Paternity, Zygosity, and Fetal Fraction
por: Bai, Zhaochen, et al.
Publicado: (2020)

Fetal Sex Results of Noninvasive Prenatal Testing and Differences With Ultrasonography
por: Dhamankar, Rupin, et al.
Publicado: (2020)

Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies
por: Jiang, Fuman, et al.
Publicado: (2012)

Noninvasive Prenatal Diagnosis of Fetal Trisomy 18 and Trisomy 13 by Maternal Plasma DNA Sequencing
por: Chen, Eric Z., et al.
Publicado: (2011)

Effects of SARS-CoV-2 on prenatal lung growth assessed by fetal MRI
por: Stoecklein, Sophia, et al.
Publicado: (2022)

Amniocentesis and Next Generation Sequencing (NGS)-Based Noninvasive Prenatal DNA Testing (NIPT) for Prenatal Diagnosis of Fetal Chromosomal Disorders
por: Qi, Qi-Ge, et al.
Publicado: (2021)

Whole-exome sequencing applications in prenatal diagnosis of fetal bowel dilatation
por: Bian, Xinyi, et al.
Publicado: (2023)

Evidence for feasibility of fetal trophoblastic cell‐based noninvasive prenatal testing
por: Breman, Amy M., et al.
Publicado: (2016)

Noninvasive prenatal testing detects microdeletion abnormalities of fetal chromosome 15
por: Yin, Lianli, et al.
Publicado: (2019)

Clinical application of noninvasive prenatal testing in the detection of fetal chromosomal diseases
por: Pang, Yu, et al.
Publicado: (2021)

Noninvasive prenatal diagnosis targeting fetal nucleated red blood cells
por: Chen, Yanyu, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_gs69hu630u0409d0o7tdlls87j