Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

scientific article published on 15 January 2016

Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations is …
instance of (P31):
scholarly articleQ13442814

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P356DOI10.1002/PD.4777
P8608Fatcat IDrelease_2iduex4n5fb2bjd4bvzbob4pye
P698PubMed publication ID26774010

P50authorBrigitte H. W. FaasQ130284899
P2093author name stringKornelia Neveling
Ingrid Gomes
Simone van den Heuvel
Lean Beulen
Hanneke Mieloo
Djie Tjwan Thung
Ellen Kater-Baats
Irma Derks-Prinsen
Wendy van Rens-Buijsman
P2860cites workDNA Sequencing versus Standard Prenatal Aneuploidy ScreeningQ22250872
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Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasmaQ33360224
Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencingQ33665399
Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencingQ34256640
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis.Q34385131
Feasibility study of semiconductor sequencing for noninvasive prenatal detection of fetal aneuploidyQ34567793
Analysis of cell-free DNA in maternal blood in screening for fetal aneuploidies: updated meta-analysisQ35552815
Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomyQ36406163
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
Introducing WISECONDOR for noninvasive prenatal diagnosticsQ38211988
Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratoriesQ38262952
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.Q40028555
Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipunctureQ43804527
Noninvasive detection of a balanced fetal translocation from maternal plasmaQ44233638
Clinical application of massively parallel sequencing-based prenatal noninvasive fetal trisomy test for trisomies 21 and 18 in 11,105 pregnancies with mixed risk factorsQ46446186
Successful noninvasive trisomy 18 detection using single molecule sequencing.Q46986331
Size distributions of maternal and fetal DNA in maternal plasma.Q47432593
Theoretical performance of non-invasive prenatal testing for chromosome imbalances using counting of cell-free DNA fragments in maternal plasma.Q50674465
Circulating fetal cell-free DNA fractions differ in autosomal aneuploidies and monosomy X.Q51163080
Comparison of the performance of Ion Torrent chips in noninvasive prenatal trisomy detection.Q51514162
Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21.Q53063252
Single molecule sequencing of free DNA from maternal plasma for noninvasive trisomy 21 detection.Q53094776
Delivering noninvasive prenatal testing in a clinical setting using semiconductor sequencing platform.Q53516393
Presence of fetal DNA in maternal plasma and serumQ57075132
Non-invasive prenatal diagnosis of fetal aneuploidies using massively parallel sequencing-by-ligation and evidence that cell-free fetal DNA in the maternal plasma originates from cytotrophoblastic cellsQ57079533
P433issue3
P304page(s)216-223
P577publication date2016-01-15
P1433published inPrenatal DiagnosisQ15760059
P1476titleValidation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations
P478volume36

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Q33845848Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomaliescites workP2860

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