Rchr
J-GLOBAL ID：201801012476719603
Update date: Oct. 30, 2024
Aoto Saki
アオト サキ | Aoto Saki
Affiliation and department：
Job title：
研究員
Research field (2)：
Genomics
, Molecular biology
Research theme for competitive and other funds (4)：
- 2020 - 2025 小児がん及びヒト多能性幹細胞に対する畳込ニューラルネットワークによる分類器の創成
- 2021 - 2024 ヒト集団におけるレトロトランスポジションの発生頻度とその発生機序の解明
- 2019 - 2020 エクソームデータを用いた大規模レトロトランスポジション検出法の開発
- 2017 - 2018 成育ゲノム医療の推進に向けたデータベース開発
Papers (11)：
-
Jonghyun Kim, Fuzuki Mizuno, Takayuki Matsushita, Masami Matsushita, Saki Aoto, Koji Ishiya, Mami Kamio, Izumi Naka, Michiko Hayashi, Kunihiko Kurosaki, et al. Genetic analysis of a Yayoi individual from the Doigahama site provides insights into the origins of immigrants to the Japanese Archipelago. Journal of Human Genetics. 2024
-
Erina Suzuki, Kazuhiko Nakabayashi, Saki Aoto, Tsutomu Ogata, Yoko Kuroki, Mami Miyado, Maki Fukami, Keiko Matsubara. DNA methylation changes in the genome of patients with hypogonadotropic hypogonadism. Heliyon. 2024. 10. 18. e37648
-
Matsubara K, Ohgami Y, Okamura K, Aoto S, Fukami M, Shimada Y. Machine learning trial to detect sex differences in simple sticker arts of 1606 preschool children. Minerva Pediatr. 2024. 76. 3. 343-349
-
Kosuke Taniguchi, Fuyuki Hasegawa, Yuka Okazaki, Asuka Hori, Hiroko Ogata-Kawata, Saki Aoto, Osuke Migita, Tomoko Kawai, Kazuhiko Nakabayashi, Kohji Okamura, et al. Re-evaluation of whole exome sequencing, including intronic region, in combination with genetic intolerance score for detecting foetal structural anomalies in X-linked disorders. 2023
-
Hidetaka Uryu, Ohsuke Migita, Minami Ozawa, Chikako Kamijo, Saki Aoto, Kohji Okamura, Fuyuki Hasegawa, Torayuki Okuyama, Motomichi Kosuga, Kenichiro Hata. Automated urinary sediment detection for Fabry disease using deep-learning algorithms. Molecular Genetics and Metabolism Reports. 2022. 33. 100921-100921
ｍore...
MISC (9)：
Lectures and oral presentations (2)：
-
Characterization of promoter sequences using relative positions of oligonucleotides and convolutional neural networks
(2018)
-
Noonan症候群様症状を示す一卵性双生児の全ゲノム解析
(2017)
Professional career (1)：
Association Membership(s) (1)：
THE MOLECULAR BIOLOGY SOCIETY OF JAPAN
