REFERENCES
1. Van den Veyver IB, Beaudet AL. Comparative genomic hybridization and prenatal diagnosis. Curr Opin Obstet Gynecol 2006;18:185-91.
3. Lo YMD, Corbetta N, Chamberlain PF, et al. Presence of fetal DNA in maternal plasma and serum. Lancet 1997;350:485-7.
5. Alberry M, Maddocks D, Jones M, et al. Free fetal DNA in maternal plasma in anembryonic pregnancies: confirmation that the origin is the trophoblast. Prenat Diagn 2007;27:415-8.
6. Rong Y, Gao J, Jiang X, Zheng F. Multiplex PCR for 17 Y-chromosome specific short tandem repeats (STR) to enhance the reliability of fetal sex determination in maternal plasma. Int J Mol Sci 2012;13:5972-81.
7. Zhang S, Han S, Zhang M, Wang Y. Non-invasive prenatal paternity testing using cell-free fetal DNA from maternal plasma: DNA isolation and genetic marker studies. Leg Med 2018;32:98-103.
8. Christiansen SL, Jakobsen B, Børsting C, et al. Non-invasive prenatal paternity testing using a standard forensic genetic massively parallel sequencing assay for amplification of human identification SNPs. Int J Legal Med 2019;133:1361-8.
9. Hu J, Yan K, Jin P, Yang Y, Sun Y, Dong M. Prenatal diagnosis of trisomy 8 mosaicism, initially identified by cffDNA screening. Mol Cytogenet 2022;15:39.
10. Juvet LK, Ormstad SS, Stoinska-Schneider A, et al. Non-invasive prenatal test (NIPT) for identification of trisomy 21, 18 and 13: report from the Norwegian Institute of Public Health No. 2016-18. 2016.
11. Butler JM. Genetics and genomics of core short tandem repeat loci used in human identity testing. J Forensic Sci 2006;51:253-65.
12. Wagner J, Dzijan S, Marjanović D, Lauc G. Non-invasive prenatal paternity testing from maternal blood. Int J Legal Med 2009;123:75-9.
13. Zhang R, Tan Y, Wang L, et al. Set of 15 SNP-SNP markers for detection of unbalanced degraded DNA mixtures and noninvasive prenatal paternity testing. Front Genet 2021;12:800598.
14. Shen X, Li R, Li H, et al. Noninvasive prenatal paternity testing with a combination of well-established SNP and STR markers using massively parallel sequencing. Genes 2021;12:454.
15. Chang L, Yu H, Miao X, Zhang J, Li S. Development and comprehensive evaluation of a noninvasive prenatal paternity testing method through a scaled trial. Forensic Sci Int Genet 2019;43:102158.
16. Gill P. An assessment of the utility of single nucleotide polymorphisms (SNPs) for forensic purposes. Int J Legal Med 2001;114:204-10.
17. Moriot A, Hall D. Analysis of fetal DNA in maternal plasma with markers designed for forensic DNA mixture resolution. Genet Med 2019;21:613-21.
18. Ou X, Qu N. Noninvasive prenatal paternity testing by target sequencing microhaps. Forensic Sci Int Genet 2020;48:102338.
19. Giannico R, Forlani L, Andrioletti V, et al. NIPAT as non-invasive prenatal paternity testing using a panel of 861 SNVs. Genes 2023;14:312.
20. Chen P, Deng C, Li Z, et al. A microhaplotypes panel for massively parallel sequencing analysis of DNA mixtures. Forensic Sci Int Genet 2019;40:140-9.
21. Chiu RWK, Poon LLM, Lau TK, Leung TN, Wong EMC, Lo YMD. Effects of blood-processing protocols on fetal and total DNA quantification in maternal plasma. Clin Chem 2001;47:1607-13.
22. Zheng H, Tao R, Zhang J, et al. Development and validation of a novel SiFaSTRTM 23-plex system. Electrophoresis 2019;40:2644-54.
23. McKenna A, Hanna M, Banks E, et al. The genome analysis Toolkit: a MapReduce framework for analyzing next-generation DNA sequencing data. Genome Res 2010;20:1297-303.
24. Li H, Durbin R. Fast and accurate short read alignment with Burrows-Wheeler transform. Bioinformatics 2009;25:1754-60.
25. Li H, Handsaker B, Wysoker A, et al. The sequence alignment/map format and SAMtools. Bioinformatics 2009;25:2078-9.
26. Baur MP, Elston RC, Gürtler H, et al. No fallacies in the formulation of the paternity index. Am J Hum Genet 1986;39:528-36.
27. Lo YMD, Patel P, Baigent CN, et al. Prenatal sex determination from maternal peripheral blood using the polymerase chain reaction. Hum Genet 1993;90:483-8.
28. Butler JM. Recent developments in Y-short tandem repeat and Y-single nucleotide polymorphism analysis. Forensic Sci Rev 2003;15:91-111.
29. Xu H, Wang S, Ma LL, et al. Informative priors on fetal fraction increase power of the noninvasive prenatal screen. Genet Med 2018;20:817-24.
30. Zaki-Dizaji M, Shafiee A, Kohandel Gargari O, Fathi H, Heidary Z. Maternal and fetal factors affecting cell-free fetal DNA (cffDNA) fraction: a systematic review. J Reprod Infertil 2023;24:219-31.
31. Birch L, English CA, O'Donoghue K, Barigye O, Fisk NM, Keer JT. Accurate and robust quantification of circulating fetal and total DNA in maternal plasma from 5 to 41 weeks of gestation. Clin Chem 2005;51:312-20.
32. Moray N, Pink KE, Borry P, Larmuseau MHD. Paternity testing under the cloak of recreational genetics. Eur J Hum Genet 2017;25:768-70.
33. Toya W. Ethical, legal and social issues in Japan on the determination of blood relationship via DNA testing. Asian Bioeth Rev 2017;9:19-32.