| scholarly article | Q13442814 |
| P50 | author | Jaroslav Budis | Q89994987 |
| Juraj Gazdarica | Q92128103 | ||
| P2093 | author name string | Jan Turna | |
| Tomas Szemes | |||
| Frantisek Duris | |||
| P2860 | cites work | Ultrafast and memory-efficient alignment of short DNA sequences to the human genome | Q21183894 |
| Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood | Q24657306 | ||
| Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
| Application of risk score analysis to low-coverage whole genome sequencing data for the noninvasive detection of trisomy 21, trisomy 18, and trisomy 13. | Q31011773 | ||
| Noninvasive prenatal diagnosis of common aneuploidies by semiconductor sequencing | Q33665399 | ||
| Size-based molecular diagnostics using plasma DNA for noninvasive prenatal testing. | Q33767643 | ||
| Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. | Q34385131 | ||
| Non-invasive prenatal assessment of trisomy 21 by multiplexed maternal plasma DNA sequencing: large scale validity study | Q34482155 | ||
| Utilization of Benchtop Next Generation Sequencing Platforms Ion Torrent PGM and MiSeq in Noninvasive Prenatal Testing for Chromosome 21 Trisomy and Testing of Impact of In Silico and Physical Size Selection on Its Analytical Performance. | Q35869114 | ||
| Cell-free fetal DNA in maternal blood: kinetics, source and structure | Q35966472 | ||
| Procedure-related complications of amniocentesis and chorionic villous sampling: a systematic review | Q36927303 | ||
| Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma | Q37010246 | ||
| WISECONDOR: detection of fetal aberrations from shallow sequencing maternal plasma based on a within-sample comparison scheme. | Q37631891 | ||
| Optimal detection of fetal chromosomal abnormalities by massively parallel DNA sequencing of cell-free fetal DNA from maternal blood | Q44645735 | ||
| Noninvasive prenatal diagnosis of common fetal chromosomal aneuploidies by maternal plasma DNA sequencing. | Q46892061 | ||
| Detection of fetal subchromosomal abnormalities by sequencing circulating cell-free DNA from maternal plasma. | Q50955444 | ||
| Presence of fetal DNA in maternal plasma and serum | Q57075132 | ||
| Combining count- and length-based z-scores leads to improved predictions in non-invasive prenatal testing | Q57157103 | ||
| Noninvasive detection of fetal trisomy 21 by sequencing of DNA in maternal blood: a study in a clinical setting | Q83395075 | ||
| Genome-wide fetal aneuploidy detection by maternal plasma DNA sequencing | Q84195901 | ||
| The importance of determining the limit of detection of non-invasive prenatal testing methods | Q87165803 | ||
| Non-invasive prenatal testing as a valuable source of population specific allelic frequencies | Q91756381 | ||
| P275 | copyright license | Creative Commons Attribution 4.0 International | Q20007257 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 14 | |
| P577 | publication date | 2019-07-11 | |
| P1433 | published in | International Journal of Molecular Sciences | Q3153277 |
| P1476 | title | Adaptable Model Parameters in Non-Invasive Prenatal Testing Lead to More Stable Predictions | |
| P478 | volume | 20 |
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