Introducing WISECONDOR for noninvasive prenatal diagnostics

scientific article published on 16 May 2014

Introducing WISECONDOR for noninvasive prenatal diagnostics is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1586/14737159.2014.919855
P698PubMed publication ID24831532

P2093author name stringErik A Sistermans
Marcel J T Reinders
Roy Straver
P2860cites workDNA Sequencing versus Standard Prenatal Aneuploidy ScreeningQ22250872
Quantification of Fetal DNA by Use of Methylation-Based DNA DiscriminationQ30987480
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.Q34385131
Noninvasive detection of fetal subchromosome abnormalities via deep sequencing of maternal plasmaQ36595101
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasmaQ37010246
WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme.Q37631891
Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal bloodQ44645735
Presence of fetal DNA in maternal plasma and serumQ57075132
P433issue5
P304page(s)513-515
P577publication date2014-05-16
P1433published inExpert Review of Molecular Diagnostics: new diagnostic technologies are set to revolutionise healthcareQ15756305
P1476titleIntroducing WISECONDOR for noninvasive prenatal diagnostics
P478volume14

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cites work (P2860)
Q33845848Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies
Q36312158Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing
Q38728695Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration.
Q37412801Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory
Q36184534Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening
Q26764809Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues
Q48274405The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies
Q38410274Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

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