| P50 | author | Angela N Barrett | Q50461436 |
| P2093 | author name string | Rui Hua | |
| | Richie Soong | |
| | Li Xiong | |
| | Niranjan Nagarajan | |
| | Arijit Biswas | |
| | Mahesh Choolani | |
| | Tuan Z Tan | |
| | Henna V Advani | |
| | Cecille Laureano-Asibal | |
| P2860 | cites work | Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts. | Q51025463 |
| | Debates on fetal fraction measurement and DNA-based noninvasive prenatal screening: time for standardisation? | Q51810585 |
| | Influence of temperature during transportation on cell-free DNA analysis. | Q53191016 |
| | A new methodology to preserve the original proportion and integrity of cell-free fetal DNA in maternal plasma during sample processing and storage. | Q53334658 |
| | Quantification of cell free fetal DNA in maternal plasma in normal pregnancies and in pregnancies with placental dysfunction. | Q53426252 |
| | Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. | Q54574187 |
| | The impact of maternal plasma DNA fetal fraction on next generation sequencing tests for common fetal aneuploidies. | Q54708648 |
| | Presence of fetal DNA in maternal plasma and serum | Q57075132 |
| | Cell-free DNA is more sensitive than cell-free mRNA as a marker for evaluation of fetal-maternal hemorrhage | Q79306207 |
| | Comparing methods for fetal fraction determination and quality control of NIPT samples. | Q38754608 |
| | Cell-free DNA fetal fraction and preterm birth | Q38908291 |
| | Multiplex digital PCR: breaking the one target per color barrier of quantitative PCR. | Q39541230 |
| | Noninvasive prenatal diagnosis of hemophilia by microfluidics digital PCR analysis of maternal plasma DNA. | Q39967854 |
| | Digital PCR analysis of maternal plasma for noninvasive detection of sickle cell anemia | Q40028010 |
| | 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 |
| | Multiplex picodroplet digital PCR to detect KRAS mutations in circulating DNA from the plasma of colorectal cancer patients. | Q40130589 |
| | Improved base calling for the Illumina Genome Analyzer using machine learning strategies | Q42558307 |
| | Noninvasive prenatal methylomic analysis by genomewide bisulfite sequencing of maternal plasma DNA. | Q44160249 |
| | FetalQuantSD: accurate quantification of fetal DNA fraction by shallow-depth sequencing of maternal plasma DNA. | Q47093534 |
| | FetalQuant: deducing fractional fetal DNA concentration from massively parallel sequencing of DNA in maternal plasma | Q47960026 |
| | A tale of three next generation sequencing platforms: comparison of Ion Torrent, Pacific Biosciences and Illumina MiSeq sequencers | Q21266698 |
| | Update on Procedure-Related Risks for Prenatal Diagnosis Techniques | Q22241937 |
| | SNP-based non-invasive prenatal testing detects sex chromosome aneuploidies with high accuracy | Q24627800 |
| | Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci | Q24632266 |
| | The human genome browser at UCSC | Q24672361 |
| | Primer3 on the WWW for general users and for biologist programmers | Q27861030 |
| | Implementing prenatal diagnosis based on cell-free fetal DNA: accurate identification of factors affecting fetal DNA yield | Q28744238 |
| | Quantification of Fetal DNA by Use of Methylation-Based DNA Discrimination | Q30987480 |
| | Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma | Q33360224 |
| | 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 study | Q34029044 |
| | Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing | Q34256640 |
| | RAPIDR: an analysis package for non-invasive prenatal testing of aneuploidy | Q34285347 |
| | Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study | Q34482155 |
| | Universal noninvasive detection of solid organ transplant rejection | Q34794715 |
| | Performance of non-invasive prenatal testing when fetal cell-free DNA is absent | Q34996829 |
| | Circulating cell-free DNA enables noninvasive diagnosis of heart transplant rejection. | Q35078413 |
| | Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies | Q35106099 |
| | Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma | Q37000915 |
| | Human diallelic insertion/deletion polymorphisms | Q37203127 |
| | Calculating the fetal fraction for noninvasive prenatal testing based on genome-wide nucleosome profiles | Q37418057 |
| | Second generation noninvasive fetal genome analysis reveals de novo mutations, single-base parental inheritance, and preferred DNA ends. | Q37514951 |
| | Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing | Q37691066 |
| | The clinical implementation of non-invasive prenatal diagnosis for single-gene disorders: challenges and progress made | Q38099617 |
| | Can the quantity of cell-free fetal DNA predict preeclampsia: a systematic review | Q38213813 |
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 10 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | e0186771 | |
| P577 | publication date | 2017-10-30 | |
| P1433 | published in | PLOS One | Q564954 |
| P1476 | title | Measurement of fetal fraction in cell-free DNA from maternal plasma using a panel of insertion/deletion polymorphisms | |
| P478 | volume | 12 | |