| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/bioinformatics/KimKKK18 |
| P356 | DOI | 10.1093/BIOINFORMATICS/BTX728 |
| P698 | PubMed publication ID | 29126132 |
| P2093 | author name string | Sunshin Kim | |
| Minjeong Kim | |||
| Jai-Hoon Kim | |||
| Kangseok Kim | |||
| P2860 | cites work | Analysis of East Asia genetic substructure using genome-wide SNP arrays | Q21562489 |
| Noninvasive prenatal aneuploidy testing of chromosomes 13, 18, 21, X, and Y, using targeted sequencing of polymorphic loci | Q24632266 | ||
| Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
| A global reference for human genetic variation | Q25909434 | ||
| Rare-variant association analysis: study designs and statistical tests | Q26852733 | ||
| Integrating common and rare genetic variation in diverse human populations | Q29547220 | ||
| Genotype imputation | Q29614590 | ||
| Genotype imputation for genome-wide association studies | Q29614880 | ||
| Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma | Q33360224 | ||
| A reference panel of 64,976 haplotypes for genotype imputation | Q33553419 | ||
| Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing | Q33665399 | ||
| Noninvasive prenatal diagnosis of congenital adrenal hyperplasia using cell-free fetal DNA in maternal plasma | Q33682367 | ||
| Targeted massively parallel sequencing of maternal plasma DNA permits efficient and unbiased detection of fetal alleles | Q33747312 | ||
| A linear complexity phasing method for thousands of genomes | Q34237936 | ||
| The feasibility study of non-invasive fetal trisomy 18 and 21 detection with semiconductor sequencing platform | Q34374066 | ||
| Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
| Sequencing depth and coverage: key considerations in genomic analyses | Q34398440 | ||
| Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study | Q34482155 | ||
| Feasibility study of semiconductor sequencing for noninvasive prenatal detection of fetal aneuploidy | Q34567793 | ||
| Maternal plasma fetal DNA fractions in pregnancies with low and high risks for fetal chromosomal aneuploidies | Q35106099 | ||
| Comparison of two high-throughput semiconductor chip sequencing platforms in noninvasive prenatal testing for Down syndrome in early pregnancy | Q36003623 | ||
| An adaptive detection method for fetal chromosomal aneuploidy using cell-free DNA from 447 Korean women | Q36157384 | ||
| Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
| Implementation of non-invasive prenatal testing by semiconductor sequencing in a genetic laboratory | Q37412801 | ||
| Bioinformatics Approaches for Fetal DNA Fraction Estimation in Noninvasive Prenatal Testing | Q37691066 | ||
| Next-generation genotype imputation service and methods | Q40603492 | ||
| 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 | ||
| Determination of fetal DNA fraction from the plasma of pregnant women using sequence read counts. | Q51025463 | ||
| Open source non-invasive prenatal testing platform and its performance in a public health laboratory. | Q51407385 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | imputation | Q1660484 |
| P577 | publication date | 2017-11-08 | |
| P1433 | published in | Bioinformatics | Q4914910 |
| P1476 | title | Cost-effective and accurate method of measuring fetal fraction using SNP imputation |
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