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.

scientific article published on 14 January 2016

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. is …
instance of (P31):
scholarly articleQ13442814

External links are
P819ADS bibcode2016PLoSO..1146997X
P356DOI10.1371/JOURNAL.PONE.0146997
P932PMC publication ID4713075
P698PubMed publication ID26765738
P5875ResearchGate publication ID290442967

P50authorXue-Xi YangQ87077651
P2093author name stringJun Zhang
Ming Li
Qi Tian
Fen-Xia Li
Ying-Song Wu
Hai-Yan Gan
Rong-Liang Liang
Xu-Ping Xu
P2860cites workDNA Sequencing versus Standard Prenatal Aneuploidy ScreeningQ22250872
DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative studyQ30414408
Quantification of Fetal DNA by Use of Methylation-Based DNA DiscriminationQ30987480
Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasmaQ33360224
Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal allelesQ33747312
Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.Q33767643
Quantification of cell-free DNA in normal and complicated pregnancies: overcoming biological and technical issuesQ33838434
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation studyQ34029044
Non-invasive prenatal chromosomal aneuploidy testing--clinical experience: 100,000 clinical samplesQ34301776
High-resolution profiling of fetal DNA clearance from maternal plasma by massively parallel sequencing.Q34340492
The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platformQ34374066
High resolution size analysis of fetal DNA in the urine of pregnant women by paired-end massively parallel sequencingQ34464967
Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity studyQ34482155
Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidiesQ35106099
Feasibility of noninvasive prenatal testing for common fetal aneuploidies in an early gestational windowQ35304735
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility studyQ36538133
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasmaQ37010246
Screening for fetal aneuploidies at 11 to 13 weeksQ37826399
ACMG statement on noninvasive prenatal screening for fetal aneuploidy.Q38096182
Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA.Q39967854
Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal DiagnosisQ46945516
Analysis of the size distributions of fetal and maternal cell-free DNA by paired-end sequencingQ47427812
Size distributions of maternal and fetal DNA in maternal plasma.Q47432593
FetalQuant: deducing fractional fetal DNA concentration from massively parallel sequencing of DNA in maternal plasmaQ47960026
Validation of ambiguous MLPA results by targeted next-generation sequencing discloses a nonsense mutation in the DMD gene.Q51136384
Non-Invasive Chromosomal Evaluation (NICE) Study: results of a multicenter prospective cohort study for detection of fetal trisomy 21 and trisomy 18.Q51349861
Clinical evaluations of cell-free fetal DNA quantities in pre-eclamptic pregnancies.Q54285680
[Comparison of EGFR mutation status in paired pre- and post-chemotherapy serum for advanced pulmonary adenocarcinoma].Q54611055
Presence of fetal DNA in maternal plasma and serumQ57075132
Fetal fraction in maternal plasma cell-free DNA at 11-13 weeks' gestation: relation to maternal and fetal characteristicsQ61847812
Fetal Fraction in Maternal Plasma Cell-Free DNA at 11–13 Weeks’ Gestation: Effect of Maternal and Fetal FactorsQ61847823
Effects of blood-processing protocols on fetal and total DNA quantification in maternal plasmaQ74403995
Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical settingQ83395075
Committee Opinion No. 545: Noninvasive prenatal testing for fetal aneuploidyQ85495453
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P4510describes a project that usesmassive parallel sequencingQ6784807
P433issue1
P407language of work or nameEnglishQ1860
P304page(s)e0146997
P577publication date2016-01-14
P1433published inPLOS OneQ564954
P1476titleA Method to Quantify Cell-Free Fetal DNA Fraction in Maternal Plasma Using Next Generation Sequencing: Its Application in Non-Invasive Prenatal Chromosomal Aneuploidy Detection
P478volume11

Reverse relations

cites work (P2860)
Q92236228A new set of DIP-SNP markers for detection of unbalanced and degraded DNA mixtures
Q64055782An enrichment method to increase cell-free fetal DNA fraction and significantly reduce false negatives and test failures for non-invasive prenatal screening: a feasibility study
Q64107192Comparison of Efficiencies of Non-invasive Prenatal Testing, Karyotyping, and Chromosomal Micro-Array for Diagnosing Fetal Chromosomal Anomalies in the Second and Third Trimesters
Q90461263Development of a comprehensive noninvasive prenatal test
Q59792872Enrichment of the fetal fraction in non-invasive prenatal screening reduces maternal background interference
Q55116442Evaluation of a novel non-invasive preimplantation genetic screening approach.
Q48276430Haplotype-based Noninvasive Prenatal Diagnosis of Hyperphenylalaninemia through Targeted Sequencing of Maternal Plasma.
Q64272413Next-generation sequencing and its clinical application

Search more.