Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System
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Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System. / Simayijiang, Halimureti; Morling, Niels; Børsting, Claus.
In: Forensic Sciences Research, Vol. 7, No. 2, 2022, p. 154-162.Research output: Contribution to journal › Journal article › Research › peer-review
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TY - JOUR
T1 - Sequencing of human identification markers in an Uyghur population using the MiSeq FGxTM Forensic Genomics System
AU - Simayijiang, Halimureti
AU - Morling, Niels
AU - Børsting, Claus
N1 - © 2020 The Author(s). Published by Taylor & Francis Group on behalf of the Academy of Forensic Science.
PY - 2022
Y1 - 2022
N2 - Massively parallel sequencing (MPS) offers a useful alternative to capillary electrophoresis (CE) based analysis of human identification markers in forensic genetics. By sequencing short tandem repeats (STRs) instead of determining the fragment lengths by CE, the sequence variation within the repeat region and the flanking regions may be identified. In this study, we typed 264 Uyghur individuals using the MiSeq FGx™ Forensic Genomics System and Primer Mix A of the ForenSeq™ DNA Signature Prep Kit that amplifies 27 autosomal STRs, 25 Y-STRs, seven X-STRs, and 94 HID-SNPs. STRinNGS v.1.0 and GATK 3.6 were used to analyse the STR regions and HID-SNPs, respectively. Increased allelic diversity was observed for 33 STRs with the PCR-MPS assay. The largest increases were found in DYS389II and D12S391, where the numbers of sequenced alleles were 3-4 times larger than those of alleles determined by repeat length alone. A relatively large number of flanking region variants (28 SNPs and three InDels) were observed in the Uyghur population. Seventeen of the flanking region SNPs were rare, and 12 of these SNPs had no accession number in dbSNP. The combined mean match probability and typical paternity index based on 26 sequenced autosomal STRs were 3.85E-36 and 1.49E + 16, respectively. This was 10 000 times lower and 1 000 times higher, respectively, than the same parameters calculated from STR repeat lengths.Key PointsSequencing data on STRs and SNPs used for human identification are presented for the Uyghur population.STRinNGS v.1.0 was used to analyse the flanking regions of STRs.The concordance between PCR-CE and PCR-MPS results was 99.86%.Detection of sequence variation in STRs and their flanking regions increased the allelic diversity.
AB - Massively parallel sequencing (MPS) offers a useful alternative to capillary electrophoresis (CE) based analysis of human identification markers in forensic genetics. By sequencing short tandem repeats (STRs) instead of determining the fragment lengths by CE, the sequence variation within the repeat region and the flanking regions may be identified. In this study, we typed 264 Uyghur individuals using the MiSeq FGx™ Forensic Genomics System and Primer Mix A of the ForenSeq™ DNA Signature Prep Kit that amplifies 27 autosomal STRs, 25 Y-STRs, seven X-STRs, and 94 HID-SNPs. STRinNGS v.1.0 and GATK 3.6 were used to analyse the STR regions and HID-SNPs, respectively. Increased allelic diversity was observed for 33 STRs with the PCR-MPS assay. The largest increases were found in DYS389II and D12S391, where the numbers of sequenced alleles were 3-4 times larger than those of alleles determined by repeat length alone. A relatively large number of flanking region variants (28 SNPs and three InDels) were observed in the Uyghur population. Seventeen of the flanking region SNPs were rare, and 12 of these SNPs had no accession number in dbSNP. The combined mean match probability and typical paternity index based on 26 sequenced autosomal STRs were 3.85E-36 and 1.49E + 16, respectively. This was 10 000 times lower and 1 000 times higher, respectively, than the same parameters calculated from STR repeat lengths.Key PointsSequencing data on STRs and SNPs used for human identification are presented for the Uyghur population.STRinNGS v.1.0 was used to analyse the flanking regions of STRs.The concordance between PCR-CE and PCR-MPS results was 99.86%.Detection of sequence variation in STRs and their flanking regions increased the allelic diversity.
KW - ForenSeq™ DNA Signature Prep Kit
KW - forensic genetics
KW - Forensic sciences
KW - Massively parallel sequencing (MPS)
KW - short tandem repeat (STR)
KW - single nucleotide polymorphism (SNP)
KW - Uyghur
U2 - 10.1080/20961790.2020.1779967
DO - 10.1080/20961790.2020.1779967
M3 - Journal article
C2 - 35784409
AN - SCOPUS:85090462569
VL - 7
SP - 154
EP - 162
JO - Forensic Sciences Research
JF - Forensic Sciences Research
SN - 2096-1790
IS - 2
ER -
ID: 258494427