scholarly article | Q13442814 |
P50 | author | Yixue Li | Q66987732 |
Yi-Lei Zhao | Q90288525 | ||
P2093 | author name string | Yan Mao | |
Haibo Li | |||
Hong Li | |||
Ting Wang | |||
Bo Liang | |||
Quanze He | |||
Jingjing Shen | |||
Lingyin Kong | |||
Yingying Xia | |||
Liming Xuan | |||
P2860 | cites work | Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts. | Q51025463 |
The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies. | Q54708648 | ||
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Probabilistic method for detecting copy number variation in a fetal genome using maternal plasma sequencing | Q33760408 | ||
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Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study | Q34482155 | ||
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Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | Q37000915 | ||
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An Optimized Method for Accurate Fetal Sex Prediction and Sex Chromosome Aneuploidy Detection in Non-Invasive Prenatal Testing | Q37115493 | ||
Size-selective separation and overall-amplification of cell-free fetal DNA fragments using PCR-based enrichment. | Q37593355 | ||
Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA. | Q39967854 | ||
Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood | Q44645735 | ||
A unified approach to risk assessment for fetal aneuploidies | Q44968322 | ||
Microsystem for isolation of fetal DNA from maternal plasma by preparative size separation | Q47172890 | ||
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma | Q47391690 | ||
Size separation of circulatory DNA in maternal plasma permits ready detection of fetal DNA polymorphisms | Q47423342 | ||
Analysis of the size distributions of fetal and maternal cell-free DNA by paired-end sequencing | Q47427812 | ||
P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 1 | |
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 17675 | |
P577 | publication date | 2018-12-05 | |
P1433 | published in | Scientific Reports | Q2261792 |
P1476 | title | Enrichment of the fetal fraction in non-invasive prenatal screening reduces maternal background interference | |
P478 | volume | 8 |
Q98291733 | A Novel Graphic-Aided Algorithm (gNIPT) Improves the Accuracy of Noninvasive Prenatal Testing |
Q89660275 | Cell-Free Fetal DNA Increases Prior to Labor at Term and in a Subset of Preterm Births |
Q102061414 | High-throughput fetal fraction amplification increases analytical performance of noninvasive prenatal screening |
Q92512130 | Sequencing of short cfDNA fragments in NIPT improves fetal fraction with higher maternal BMI and early gestational age |
Q64066279 | The Effect of Freezing on Non-invasive Prenatal Testing |
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