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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.
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 October 11, 2024)