scholarly article | Q13442814 |
P2093 | author name string | Hao Sun | |
Kun Sun | |||
Peiyong Jiang | |||
Rossa W K Chiu | |||
Tak Y Leung | |||
Xiaoxi Su | |||
Yuk Ming Dennis Lo | |||
Kwan Chee Allen Chan | |||
Stephanie C Y Yu | |||
Weng In Chu | |||
Xianlu Peng | |||
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DNA sequencing of maternal plasma reliably identifies trisomy 18 and trisomy 13 as well as Down syndrome: an international collaborative study | Q30414408 | ||
Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma | Q33360224 | ||
Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma | Q33682367 | ||
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Noninvasive prenatal testing goes global | Q33957923 | ||
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Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. | Q54574187 | ||
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Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
Non-invasive prenatal diagnosis by single molecule counting technologies | Q37525261 | ||
Noninvasive prenatal diagnosis of duchenne muscular dystrophy: comprehensive genetic diagnosis in carrier, proband, and fetus | Q39020995 | ||
Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA. | Q39967854 | ||
Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18. | Q40028555 | ||
Noninvasive prenatal diagnosis of monogenic diseases by targeted massively parallel sequencing of maternal plasma: application to β-thalassemia. | Q40057027 | ||
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Investigating single nucleotide polymorphism (SNP) density in the human genome and its implications for molecular evolution | Q48233191 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P304 | page(s) | 16013 | |
P577 | publication date | 2016-05-11 | |
P1433 | published in | NPJ genomic medicine | Q27727516 |
P1476 | title | FetalQuantSD: accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA. | |
P478 | volume | 1 |
Q37691066 | Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing |
Q92642536 | Combination of Fetal Fraction Estimators Based on Fragment Lengths and Fragment Counts in Non-Invasive Prenatal Testing |
Q47308150 | Cost-effective and accurate method of measuring fetal fraction using SNP imputation |
Q91846514 | Development of a new methylation-based fetal fraction estimation assay using multiplex ddPCR |
Q90689839 | Enrichment of fetal and maternal long cell-free DNA fragments from maternal plasma following DNA repair |
Q92995881 | Inferring fetal fractions from read heterozygosity empowers the noninvasive prenatal screening |
Q47130174 | Measurement of fetal fraction in cell-free DNA from maternal plasma using a panel of insertion/deletion polymorphisms |
Q92895469 | PREFACE: In silico pipeline for accurate cell-free fetal DNA fraction prediction |
Q64983063 | Recent trends in prenatal genetic screening and testing. |
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