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Massively parallel sequencing data of 31 autosomal STR loci obtained using the Precision ID GlobalFiler NGS STR Panel v2 for 82 Japanese population samples

Published

Author(s)

Tetsushi Kitayama, Kevin Kiesler, Takashi Fukagawa, Haruhiko Watahiki, Yusuke Mita, Koji Fujii, Kazumasa Sekiguchi, Peter Vallone, Natsuko Mizuno

Abstract

Allele frequencies for 31 autosomal short tandem repeat (STR) loci (CSF1PO, D10S1248, D12ATA63, D12S391, D13S317, D14S1434, D16S539, D18S51, D19S433, D1S1656, D1S1677, D21S11, D22S1045, D2S1338, D2S1776, D2S441, D3S1358, D3S4529, D4S2408, D5S2800, D5S818, D6S1043, D6S474, D7S820, D8S1179, FGA, Penta D, Penta E, TH01, TPOX, and vWA) were obtained using Precision ID GlobalFiler NGS STR Panel v2 from 82 unrelated individuals sampled from the Japanese population. Autosomal STR alleles designated by NGS and conventional capillary electrophoresis were found to be concordant except at D2S441 allele 9.
Citation
Legal Medicine

Keywords

Allele frequency, Japanese, Population data, Precision ID GlobalFiler NGS STR Panel v2, Short tandem repeat

Citation

Kitayama, T. , Kiesler, K. , Fukagawa, T. , Watahiki, H. , Mita, Y. , Fujii, K. , Sekiguchi, K. , Vallone, P. and Mizuno, N. (2022), Massively parallel sequencing data of 31 autosomal STR loci obtained using the Precision ID GlobalFiler NGS STR Panel v2 for 82 Japanese population samples, Legal Medicine, [online], https://doi.org/10.1016/j.legalmed.2022.102082 (Accessed August 19, 2022)
Created April 29, 2022, Updated May 10, 2022