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SNP-Based Fetal DNA Detection in Maternal Serum Using the HID-Ion AmpliSeqTM Identity Panel

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초록

Fetal DNA (fDNA) detection in maternal serum is a challenge due to low copy number and the smaller size of fDNA fragments compared to DNA fragments derived from the mother. Massively parallel sequencing (MPS) is a useful technique for fetal genetic analysis that is able to detect and quantify small amounts of DNA. In this study, seven clinical samples of maternal serum potentially containing fDNA were analyzed with a commercial single nucleotide polymorphism (SNP) panel, the HID-Ion AmpliSeqTM Identity Panel, and the results were compared to those from previous studies. Reference profiles for mothers and fetuses were not available, but multiple Y chromosomal SNPs were detected in two samples, indicating that fDNA was present in the serum and thereby validating observations of autosomal SNPs. This suggests that SNP-based MPS can be valuable for fDNA detection, thereby offering an insight into fetal genetic status. This technology could also be used to detect small amounts of DNA in mixed DNA samples for forensic applications.

Abstract

Fetal DNA (fDNA) detection in maternal serum is a challenge due to low copy number and the smaller size of fDNA fragments compared to DNA fragments derived from the mother. Massively parallel sequencing (MPS) is a useful technique for fetal genetic analysis that is able to detect and quantify small amounts of DNA. In this study, seven clinical samples of maternal serum potentially containing fDNA were analyzed with a commercial single nucleotide polymorphism (SNP) panel, the HID-Ion AmpliSeqTM Identity Panel, and the results were compared to those from previous studies. Reference profiles for mothers and fetuses were not available, but multiple Y chromosomal SNPs were detected in two samples, indicating that fDNA was present in the serum and thereby validating observations of autosomal SNPs. This suggests that SNP-based MPS can be valuable for fDNA detection, thereby offering an insight into fetal genetic status. This technology could also be used to detect small amounts of DNA in mixed DNA samples for forensic applications.

참고문헌 (10)

  1. Chan KC, "Size distributions of maternal and fetal DNA in maternal plasma", Clin Chem, 50, pp.88~92 (2004)
  2. Wang E, "Gestational age and maternal weight effects on fetal cell-free DNA in maternal plasma", Prenat Diagn, 33, pp.662~666 (2013)
  3. Chitty LS, "Non-invasive prenatal diagnosis of achondroplasia and thanatophoric dysplasia: nextgeneration sequencing allows for a safer, more accurate, and comprehensive approach", Prenat Diagn, 35, pp.656~662 (2015)
  4. Borsting C, "Evaluation of the Ion Torrent™ HID SNP 169-plex: A SNP typing assay developed for human identification by second generation sequencing", Forensic Sci Int Genet, 12, pp.144~154 (2014)
  5. Eduardoff M, "Inter-laboratory evaluation of SNP-based forensic identification by massively parallel sequencing using the Ion PGM", Forensic Sci Int Genet, 17, pp.110~121 (2015)
  6. Ochiai E, "Evaluation of Y chromosomal SNP haplogrouping in the HID-Ion AmpliSeq Identity Panel", Leg Med (Tokyo), 22, pp.58~61 (2016)
  7. Buchard A, "ISO 17025 validation of a next-generation sequencing assay for relationship testing", Electrophoresis, 37, pp.2822~2831 (2016)
  8. Guo F, "Next generation sequencing of SNPs using the HID-Ion AmpliSeq Identity Panel on the Ion Torrent PGM platform", Forensic Sci Int Genet, 25, pp.73~84 (2016)
  9. Barra GB, "Fetal male lineage determination by analysis of Y-chromosome STR haplotype in maternal plasma", Forensic Sci Int Genet, 15, pp.105~110 (2015)
  10. Churchill JD, "Blind study evaluation illustrates utility of the Ion PGM system for use in human identity DNA typing", Croat Med J, 56, pp.218~229 (2015)

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