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3.5KJPNv2: an allele frequency panel of 3552 Japanese individuals including the X chromosome.
Tadaka S, Katsuoka F, Ueki M, Kojima K, Makino S, Saito S, Otsuki A, Gocho C, Sakurai-Yageta M, Danjoh I, Motoike IN, Yamaguchi-Kabata Y, Shirota M, Koshiba S, Nagasaki M, Minegishi N, Hozawa A, Kuriyama S, Shimizu A, Yasuda J, Fuse N; Tohoku Medical Megabank Project Study Group; Tamiya G, Yamamoto M, Kinoshita K. Tadaka S, et al. Among authors: nagasaki m. Hum Genome Var. 2019 Jun 18;6:28. doi: 10.1038/s41439-019-0059-5. eCollection 2019. Hum Genome Var. 2019. PMID: 31240104 Free PMC article.
Validation of multiple single nucleotide variation calls by additional exome analysis with a semiconductor sequencer to supplement data of whole-genome sequencing of a human population.
Motoike IN, Matsumoto M, Danjoh I, Katsuoka F, Kojima K, Nariai N, Sato Y, Yamaguchi-Kabata Y, Ito S, Kudo H, Nishijima I, Nishikawa S, Pan X, Saito R, Saito S, Saito T, Shirota M, Tsuda K, Yokozawa J, Igarashi K, Minegishi N, Tanabe O, Fuse N, Nagasaki M, Kinoshita K, Yasuda J, Yamamoto M. Motoike IN, et al. Among authors: nagasaki m. BMC Genomics. 2014 Aug 10;15(1):673. doi: 10.1186/1471-2164-15-673. BMC Genomics. 2014. PMID: 25109789 Free PMC article.
381 results