Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles.
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 lociNon-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsNoninvasive prenatal diagnosis of fetal trisomy 21 by allelic ratio analysis using targeted massively parallel sequencing of maternal plasma DNAHigh-throughput detection of actionable genomic alterations in clinical tumor samples by targeted, massively parallel sequencingTargeted capture enrichment and sequencing identifies extensive nucleotide variation in the turkey MHC-B.Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.From prenatal genomic diagnosis to fetal personalized medicine: progress and challenges.Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.Noninvasive twin zygosity assessment and aneuploidy detection by maternal plasma DNA sequencing.Noninvasive prenatal molecular karyotyping from maternal plasma.Determination of fetal chromosome aberrations from fetal DNA in maternal blood: has the challenge finally been met?Genetic screening.Hybridization capture using short PCR products enriches small genomes by capturing flanking sequences (CapFlank)A Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection.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 PlasmaPostnatal and non-invasive prenatal detection of β-thalassemia mutations based on Taqman genotyping assays.Array comparative genomic hybridization in prenatal diagnosis of first trimester pregnancies at high risk for chromosomal anomaliesCell-free fetal DNA testing for fetal aneuploidy and beyond: clinical integration challenges in the US contextSelective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy.Development of novel noninvasive prenatal testing protocol for whole autosomal recessive disease using picodroplet digital PCRInvestigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing.Milestones in the history of hemoglobin research (in memory of professor Titus H.J. Huisman).Plasma nucleic acid analysis by massively parallel sequencing: pathological insights and diagnostic implications.Fetal nucleic acids in maternal blood: the promises.Fetal DNA in maternal plasma: a noninvasive tool for prenatal diagnosis of beta-thalassemia.Non-invasive prenatal diagnostics using next generation sequencing: technical, legal and social challenges.Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies.Cell-free Fetal Nucleic Acid Identifier Markers in Maternal Circulation.The impact of digital DNA counting technologies on noninvasive prenatal testing.Intrauterine death in singleton pregnancies with trisomy 21, 18, 13 and monosomy X.How novel molecular diagnostic technologies and biomarkers are revolutionizing genetic testing and patient care.FetalQuantSD: accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA.Cost-effective and accurate method of measuring fetal fraction using SNP imputation.Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.Noninvasive fetal trisomy 21 detection using chromosome-selective sequencing: a variation of the molecular counting theme.Noninvasive prenatal detection of chromosomal aneuploidies using different next generation sequencing strategies and algorithms.Sensitive Monogenic Noninvasive Prenatal Diagnosis by Targeted Haplotyping.
P2860
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P2860
Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles.
description
2010 nî lūn-bûn
@nan
2010 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի նոյեմբերին հրատարակված գիտական հոդված
@hy
2010年の論文
@ja
2010年論文
@yue
2010年論文
@zh-hant
2010年論文
@zh-hk
2010年論文
@zh-mo
2010年論文
@zh-tw
2010年论文
@wuu
name
Targeted massively parallel se ...... ed detection of fetal alleles.
@ast
Targeted massively parallel se ...... ed detection of fetal alleles.
@en
type
label
Targeted massively parallel se ...... ed detection of fetal alleles.
@ast
Targeted massively parallel se ...... ed detection of fetal alleles.
@en
prefLabel
Targeted massively parallel se ...... ed detection of fetal alleles.
@ast
Targeted massively parallel se ...... ed detection of fetal alleles.
@en
P2093
P1433
P1476
Targeted massively parallel se ...... ed detection of fetal alleles.
@en
P2093
Fiona M F Lun
Gary J W Liao
K C Allen Chan
Rossa W K Chiu
Tak Y Leung
Y M Dennis Lo
Yama W L Zheng
P304
P356
10.1373/CLINCHEM.2010.154336
P407
P50
P577
2010-11-15T00:00:00Z