Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics
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Understanding the Basics of NGS: From Mechanism to Variant CallingNon-Invasive Prenatal Testing Using Cell Free DNA in Maternal Plasma: Recent Developments and Future ProspectsIdentification 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 managementDetection of chromosomal alterations in the circulation of cancer patients with whole-genome sequencingFAST-SeqS: a simple and efficient method for the detection of aneuploidy by massively parallel sequencingNoninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencingPerformance of the neoBona test: a new paired-end massively parallel shotgun sequencing approach for cell-free DNA-based aneuploidy screening.Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingNovel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing.Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies.Assessment of circulating copy number variant detection for cancer screening.The Epigenome View: An Effort towards Non-Invasive Prenatal DiagnosisAnalysis of biological features associated with meiotic recombination hot and cold spots in Saccharomyces cerevisiaeRAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy.Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study.Noninvasive Fetal Trisomy (NIFTY) test: an advanced noninvasive prenatal diagnosis methodology for fetal autosomal and sex chromosomal aneuploidies.Rapid Short-Read Sequencing and Aneuploidy Detection Using MinION Nanopore TechnologyMethods for multiplex template sampling in digital PCR assays2D DIGE analysis of maternal plasma for potential biomarkers of Down SyndromeTracking single hematopoietic stem cells in vivo using high-throughput sequencing in conjunction with viral genetic barcodingNoninvasive prenatal diagnosis: pregnant women's interest and expected uptake.An Advanced Model to Precisely Estimate the Cell-Free Fetal DNA Concentration in Maternal PlasmaStatistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number VariationImproving the Positive Predictive Value of Non-Invasive Prenatal Screening (NIPS)Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing.Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.Limited Clinical Utility of Non-invasive Prenatal Testing for Subchromosomal Abnormalities.Integration of noninvasive DNA testing for aneuploidy into prenatal care: what has happened since the rubber met the road?Non-invasive Prenatal Testing: Technologies, Clinical Assays and Implementation Strategies for Women's Healthcare Practitioners.Tumor-associated copy number changes in the circulation of patients with prostate cancer identified through whole-genome sequencing.Carrier testing for severe childhood recessive diseases by next-generation sequencingNext generation sequencing of SNPs for non-invasive prenatal diagnosis: challenges and feasibility as illustrated by an application to β-thalassaemia.NIPTRIC: an online tool for clinical interpretation of non-invasive prenatal testing (NIPT) results.Investigating and correcting plasma DNA sequencing coverage bias to enhance aneuploidy discovery.Current controversies in prenatal diagnosis 2: Down syndrome screening: is ultrasound better than cell-free nucleic acids in maternal blood?Plasma nucleic acid analysis by massively parallel sequencing: pathological insights and diagnostic implications.Fetal nucleic acids in maternal blood: the promises.Noninvasive prenatal diagnosis empowered by high-throughput sequencing.Non-invasive prenatal testing for aneuploidy: current status and future prospects.
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P2860
Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics
description
2010 nî lūn-bûn
@nan
2010 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2010 թվականի մայիսին 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
Sensitivity of noninvasive pre ...... ed only by counting statistics
@ast
Sensitivity of noninvasive pre ...... ed only by counting statistics
@en
Sensitivity of noninvasive pre ...... ed only by counting statistics
@nl
type
label
Sensitivity of noninvasive pre ...... ed only by counting statistics
@ast
Sensitivity of noninvasive pre ...... ed only by counting statistics
@en
Sensitivity of noninvasive pre ...... ed only by counting statistics
@nl
prefLabel
Sensitivity of noninvasive pre ...... ed only by counting statistics
@ast
Sensitivity of noninvasive pre ...... ed only by counting statistics
@en
Sensitivity of noninvasive pre ...... ed only by counting statistics
@nl
P2860
P3181
P1433
P1476
Sensitivity of noninvasive pre ...... ed only by counting statistics
@en
P2093
H Christina Fan
Stephen R Quake
P2860
P304
P3181
P356
10.1371/JOURNAL.PONE.0010439
P407
P577
2010-05-03T00:00:00Z