Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management - Wikidata - wikimedia - TriplyDB

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

http://www.wikidata.org/entity/Q27324761

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Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessments Statistical Approach to Decreasing the Error Rate of Noninvasive Prenatal Aneuploid Detection caused by Maternal Copy Number Variation Detection of complex deletions in chromosomes 13 and 21 in a fetus by noninvasive prenatal testing Enlarged NT (≥3.5 mm) in the first trimester - not all chromosome aberrations can be detected by NIPT.Clinical outcome of subchromosomal events detected by whole-genome noninvasive prenatal testing.Cell-free DNA testing of an extended range of chromosomal anomalies: clinical experience with 6,388 consecutive cases.Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.Comparing methods for fetal fraction determination and quality control of NIPT samples.The clinical utility of genome-wide non invasive prenatal screening.Expanding non-invasive prenatal testing beyond chromosomes 21, 18, 13, X and Y.Prenatal and pre-implantation genetic diagnosis.Should we 'open the kimono' to release the results of rare autosomal aneuploidies following noninvasive prenatal whole genome sequencing?Genomics-based non-invasive prenatal testing for detection of fetal chromosomal aneuploidy in pregnant women.Maternal liver transplant: Another cause of discordant fetal sex determination using cell-free DNA.Author's reply to Grati and Benn.Contribution of maternal copy number variations to false-positive fetal trisomies detected by noninvasive prenatal testing.Accuracy and clinical value of maternal incidental findings during noninvasive prenatal testing for fetal aneuploidies.Combination approach for detecting different types of alterations in circulating tumor DNA in leiomyosarcoma.Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test.NIPTmer: rapid k-mer-based software package for detection of fetal aneuploidies.A foetus with 18p11.32-q21.2 duplication and Xp22.33-p11.1 deletion derived from a maternal reciprocal translocation t(X;18)(q13;q21.3).Strategies to minimize false positives and interpret novel microdeletions based on maternal copy-number variants in 87,000 noninvasive prenatal screens In case you missed it: thePrenatal Diagnosiseditors bring you the most significant advances of 2015

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Noninvasive prenatal testing using a novel analysis pipeline to screen for all autosomal fetal aneuploidies improves pregnancy management

http://www.wikidata.org/entity/Q27324761

description

2015 nî lūn-bûn

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2015 թուականի Յունուարին հրատարակուած գիտական յօդուած

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2015 թվականի հունվարին հրատարակված գիտական հոդված

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年論文

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2015年论文

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Noninvasive prenatal testing u ...... improves pregnancy management

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Baran Bayindir

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Eric Legius

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Hilde Peeters

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Molka Kammoun

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An integrated encyclopedia of DNA elements in the human genome

DNA Sequencing versus Standard Prenatal Aneuploidy Screening

Fast and accurate short read alignment with Burrows-Wheeler transform

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

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

The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data

European collaborative research on mosaicism in CVS (EUCROMIC)--fetal and extrafetal cell lineages in 192 gestations with CVS mosaicism involving single autosomal trisomy

Accuracy of cytogenetic findings on chorionic villus sampling (CVS)--diagnostic consequences of CVS mosaicism and non-mosaic discrepancy in centres contributing to EUCROMIC 1986-1992

Noninvasive prenatal diagnosis of fetal trisomy 18 and trisomy 13 by maternal plasma DNA sequencing

Sensitivity of noninvasive prenatal detection of fetal aneuploidy from maternal plasma using shotgun sequencing is limited only by counting statistics

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