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Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

http://www.wikidata.org/entity/Q24657306

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Diagnostic Accuracy of Noninvasive Detection of Fetal Trisomy 21 in Maternal Blood: A Systematic Review Noninvasive detection of fetal trisomy 21: systematic review and report of quality and outcomes of diagnostic accuracy studies performed between 1997 and 2012 Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci Clinical Genetic Testing in Gastroenterology Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues Understanding the Basics of NGS: From Mechanism to Variant Calling Non-invasive prenatal diagnosis of fetal trisomy 21 using cell-free fetal DNA in maternal blood High-throughput sequencing for biology and medicine Non-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future Prospects Perinatal systemic gene delivery using adeno-associated viral vectors Free DNA--new potential analyte in clinical laboratory diagnostics?Review: cell-free fetal DNA in the maternal circulation as an indication of placental health and disease Tracking fetal development through molecular analysis of maternal biofluids Identification of trisomy 18, trisomy 13, and Down syndrome from maternal plasma Non-invasive prenatal testing for fetal chromosomal abnormalities by low-coverage whole-genome sequencing of maternal plasma DNA: review of 1982 consecutive cases in a single center Liquid biopsies: genotyping circulating tumor DNA Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management Recent advances in prenatal genetic screening and testing Skeletal dysplasias Blood-based analyses of cancer: circulating tumor cells and circulating tumor DNA Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis High-throughput droplet digital PCR system for absolute quantitation of DNA copy number Detection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencing A Non-Invasive Droplet Digital PCR (ddPCR) Assay to Detect Paternal CFTR Mutations in the Cell-Free Fetal DNA (cffDNA) of Three Pregnancies at Risk of Cystic Fibrosis via Compound Heterozygosity Single-stranded DNA library preparation uncovers the origin and diversity of ultrashort cell-free DNA in plasma FAST-SeqS: a simple and efficient method for the detection of aneuploidy by massively parallel sequencing Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing Non-invasive prenatal detection of trisomy 21 using tandem single nucleotide polymorphisms Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics The molecular evolution of acquired resistance to targeted EGFR blockade in colorectal cancers The accuracy of cell-free fetal DNA-based non-invasive prenatal testing in singleton pregnancies: a systematic review and bivariate meta-analysis.DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study.Detection and quantification of rare mutations with massively parallel sequencing.Copy-number variation and false positive prenatal aneuploidy screening results.RVD2: an ultra-sensitive variant detection model for low-depth heterogeneous next-generation sequencing data.Application of risk score analysis to low-coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13.Direct metagenomic detection of viral pathogens in nasal and fecal specimens using an unbiased high-throughput sequencing approach Using population-based data to predict the impact of introducing noninvasive prenatal diagnosis for Down syndrome.

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P2860

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

http://www.wikidata.org/entity/Q24657306

description

2008 nî lūn-bûn

@nan

2008 թուականի Հոկտեմբերին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հոտեմբերին հրատարակված գիտական հոդված

@hy

2008年の論文

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2008年論文

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2008年論文

@zh-hant

2008年論文

@zh-hk

2008年論文

@zh-mo

2008年論文

@zh-tw

2008年论文

@wuu

name

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@ast

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@en

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@nl

type

label

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@ast

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@en

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@nl

prefLabel

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@ast

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@en

Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@nl

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Proceedings of the National Academy of Sciences of the United States of America

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Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood

@en

P2093

H Christina Fan

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Louanne Hudgins

http://www.w3.org/2001/XMLSchema#string

Stephen R Quake

http://www.w3.org/2001/XMLSchema#string

Usha Chitkara

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Yair J Blumenfeld

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P2860

Initial sequencing and analysis of the human genome

Isolation of fetal DNA from nucleated erythrocytes in maternal blood

Fetal cells in the blood of pregnant women: detection and enrichment by fluorescence-activated cell sorting

A genomic code for nucleosome positioning

Next-generation DNA sequencing methods

Dynamic regulation of nucleosome positioning in the human genome

Substantial biases in ultra-short read data sets from high-throughput DNA sequencing

Fetal gender and aneuploidy detection using fetal cells in maternal blood: analysis of NIFTY I data. National Institute of Child Health and Development Fetal Cell Isolation Study.

Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection.

Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.

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105

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