S
Satoru Miyano
Researcher at Tokyo Medical and Dental University
Publications - 874
Citations - 45801
Satoru Miyano is an academic researcher from Tokyo Medical and Dental University. The author has contributed to research in topics: Gene & Gene regulatory network. The author has an hindex of 84, co-authored 811 publications receiving 38723 citations. Previous affiliations of Satoru Miyano include University of Paderborn & Institute of Medical Science.
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Identification and quantification of Granger causality between gene sets
André Fujita,João Ricardo Sato,Kaname Kojima,Luciana Rodrigues Gomes,Masao Nagasaki,Mari Cleide Sogayar,Satoru Miyano +6 more
TL;DR: The multivariate Granger causality concept is generalized in order to identify Granger causalities between sets of gene expressions, i.e., whether a set of n genes Granger-causes another set of m genes, aiming at identifying and quantifying the flow of information between gene networks (or pathways).
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Using maximal independent sets to solve problems in parallel
Takayoshi Shoudai,Satoru Miyano +1 more
TL;DR: By using an O((log n)2) time EREW PRAM algorithm for a maximal independent set problem (MIS), the maximal vertex-induced subgraph satisfying a hereditary graph property π can be found in time 0(Δλ(π)Tπ(n)(log n).2) using a polynomial number of processors.
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Genetic Predispositions to Myeloid Neoplasms Caused By Germline DDX41 Mutations
June Takeda,Kenichi Yoshida,Hideki Makishima,Tetsuichi Yoshizato,Yusuke Shiozawa,Yuichi Shiraishi,Yusuke Okuno,Ayana Kon,Yasunobu Nagata,Keisuke Kataoka,Kenichi Chiba,Hiroko Tanaka,Masashi Sanada,Mamiko Sakata-Yanagimoto,Naoshi Obara,Tsuyoshi Nakamaki,Ken Ishiyama,Akira Haigaishi,Shigeru Chiba,Hiraku Mori,Norio Asou,Hitoshi Kiyoi,Chikara Hirase,Kiyotoshi Imai,Nobuaki Dobashi,Toru Kiguchi,Yasushi Miyazaki,Tomoki Naoe,Satoru Miyano,Kensuke Usuki,Shuichi Miyawaki,Yoichiro Kamatani,Yukihide Momozawa,Michiaki Kubo,Chantana Polprasert,Jaroslaw P. Maciejewski,Seishi Ogawa +36 more
TL;DR: Germline variants of DDX41 showed significant enrichment in AML/MDS cases compared to the respective control population, although the enrichment of individual variants showed substantial variations, suggesting different effect size among these variants.
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Application of targeted nanopore sequencing for the screening and determination of structural variants in patients with Lynch syndrome.
Kiyoshi Yamaguchi,Rika Kasajima,Kiyoko Takane,Seira Hatakeyama,Eigo Shimizu,Rui Yamaguchi,Rui Yamaguchi,Kotoe Katayama,Masami Arai,Chikashi Ishioka,Takeo Iwama,Satoshi Kaneko,Nagahide Matsubara,Yoshihiro Moriya,Tadashi Nomizu,Kokichi Sugano,Kazuo Tamura,Naohiro Tomita,Teruhiko Yoshida,Kenichi Sugihara,Yusuke Nakamura,Satoru Miyano,Satoru Miyano,Seiya Imoto,Yoichi Furukawa,Tsuneo Ikenoue +25 more
TL;DR: In this paper, the authors have tested the efficacy of long read-sequencing coupled with target enrichment for the determination of structural variants of mismatch repair (MMR) genes and their breakpoints.