COFFEE: control-free noninvasive fetal chromosomal examination using maternal plasma DNA.

scientific article

COFFEE: control-free noninvasive fetal chromosomal examination using maternal plasma DNA. is …
instance of (P31):
scholarly articleQ13442814

External links are
P356DOI10.1002/PD.5016
P698PubMed publication ID28165140

P50authorKun SunQ44160284
P2093author name stringPeiyong Jiang
Rossa W K Chiu
Y M Dennis Lo
K C Allen Chan
Irena Hudecova
P2860cites workDNA Sequencing versus Standard Prenatal Aneuploidy ScreeningQ22250872
Non-invasive prenatal testing: a review of international implementation and challengesQ26999426
Prenatal Diagnosis of Fetal RhD Status by Molecular Analysis of Maternal PlasmaQ28314918
Shotgun bisulphite sequencing of the Arabidopsis genome reveals DNA methylation patterningQ29615977
Characterizing and measuring bias in sequence dataQ30635784
Plasma DNA tissue mapping by genome-wide methylation sequencing for noninvasive prenatal, cancer, and transplantation assessmentsQ30667824
Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasmaQ33682367
Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing.Q33767643
DNA sequencing of maternal plasma to detect Down syndrome: an international clinical validation studyQ34029044
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
Digital PCR for the molecular detection of fetal chromosomal aneuploidyQ35916813
Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasmaQ37000915
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasmaQ37010246
Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends.Q37514951
WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme.Q37631891
The impact of digital DNA counting technologies on noninvasive prenatal testingQ38584359
Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia.Q40057027
Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA.Q44160249
Size distributions of maternal and fetal DNA in maternal plasma.Q47432593
Maternal Plasma DNA Sequencing Reveals the Genome-Wide Genetic and Mutational Profile of the FetusQ56937251
Presence of fetal DNA in maternal plasma and serumQ57075132
P433issue4
P304page(s)336-340
P577publication date2017-02-17
P1433published inPrenatal DiagnosisQ15760059
P1476titleCOFFEE: control-free noninvasive fetal chromosomal examination using maternal plasma DNA
P478volume37

Reverse relations

cites work (P2860)
Q64077212Bayesian-based noninvasive prenatal diagnosis of single-gene disorders
Q61799424Epigenetic Biomarkers in Cell-Free DNA and Applications in Liquid Biopsy
Q64983063Recent trends in prenatal genetic screening and testing.
Q55209454Size-tagged preferred ends in maternal plasma DNA shed light on the production mechanism and show utility in noninvasive prenatal testing.
Q89849944The Length and Distribution of Plasma Cell-Free DNA Fragments in Stroke Patients
Q60929787deletion causes aberrations in length and end-motif frequencies in plasma DNA

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