Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing
about
SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracyNoninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic lociCracking the Code of Human Diseases Using Next-Generation Sequencing: Applications, Challenges, and PerspectivesSomatic mosaicism in the human genomeFree DNA--new potential analyte in clinical laboratory diagnostics?Tracking fetal development through molecular analysis of maternal biofluidsIdentification of trisomy 18, trisomy 13, and Down syndrome from maternal plasmaNoninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy managementAccuracy of non-invasive prenatal testing using cell-free DNA for detection of Down, Edwards and Patau syndromes: a systematic review and meta-analysisApplying computation biology and "big data" to develop multiplex diagnostics for complex chronic diseases such as osteoarthritisDNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessmentsSynthetic spike-in standards improve run-specific systematic error analysis for DNA and RNA sequencing.Clinical Utility of Non-Invasive Prenatal Screening from Maternal Blood.Non-invasive prenatal detection of trisomy 13 using a single nucleotide polymorphism- and informatics-based approach.Placental mosaicism for Trisomy 13: a challenge in providing the cell-free fetal DNA testingNoninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingNovel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.The Epigenome View: An Effort towards Non-Invasive Prenatal DiagnosisA new model for providing cell-free DNA and risk assessment for chromosome abnormalities in a public hospital settingDNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation study.Single-nucleotide polymorphism-based noninvasive prenatal screening in a high-risk and low-risk cohortFrom prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Six consecutive false positive cases from cell-free fetal DNA testing in a single referring centreRecent advances in the prenatal interrogation of the human fetal genome.Validation of targeted sequencing of single-nucleotide polymorphisms for non-invasive prenatal detection of aneuploidy of chromosomes 13, 18, 21, X, and Y.Noninvasive detection of cancer-associated genome-wide hypomethylation and copy number aberrations by plasma DNA bisulfite sequencingThe promise of whole-exome sequencing in medical genetics.Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.High-throughput massively parallel sequencing for fetal aneuploidy detection from maternal plasmaNoninvasive prenatal molecular karyotyping from maternal plasma.Non-invasive prenatal testing of trisomy 18 by an epigenetic marker in first trimester maternal plasma.Lengthening and shortening of plasma DNA in hepatocellular carcinoma patients.Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysis.Positive predictive value of non-invasive prenatal screening for fetal chromosome disorders using cell-free DNA in maternal serum: independent clinical experience of a tertiary referral centerBeyond Trisomy 21: Additional Chromosomal Anomalies Detected through Routine Aneuploidy Screening.Cell-free fetal DNA in the maternal circulation originates from the cytotrophoblast: proof from an unique case.Non-invasive prenatal diagnosis by massively parallel sequencing of maternal plasma DNA.An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal Plasma
P2860
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P2860
Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing
description
2011 nî lūn-bûn
@nan
2011 թուականին հրատարակուած գիտական յօդուած
@hyw
2011 թվականին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@ast
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@en
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@nl
type
label
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@ast
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@en
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@nl
prefLabel
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@ast
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@en
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@nl
P2093
P2860
P50
P3181
P1433
P1476
Noninvasive prenatal diagnosis ...... maternal plasma DNA sequencing
@en
P2093
Attie T J I Go
Cees B M Oudejans
Elizabeth T Lau
Eric Z Chen
Fiona M F Lun
Helena Lam
John M G van Vugt
K C Allen Chan
Kypros H Nicolaides
Lisa Y S Chan
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0021791
P407
P577
2011-01-01T00:00:00Z