Hideto Mori, Ph.D.

Specially Appointed Associate Professor (Full-Time), Yachie laboratory,
Premium Research Institute for Human Metaverse Medicine (PRIMe), Osaka University

Research interests

E-mail: mori.hideto.prime[at]osaka-u.ac.jp, hideto7592[at]gmail.com

GitHub: https://github.com/ponnhide

Twitter: https://twitter.com/Morihideponn

Reddit: https://www.reddit.com/user/ponnhide

Qiita: https://qiita.com/ponnhide

Education

Work Experience

Research Experiences

Publications

Selected articles

Mori H, Yachie N.
A framework to efficiently describe and share reproducible DNA materials and construction protocols.
Nature Communications. 2022 May 24;13(1):2894. 

Sakata RC, Ishiguro S, Mori H, Tanaka M, Tatsuno K, Ueda H, Yamamoto S, Seki M, Masuyama N, Nishida K, Nishimasu H, Arakawa K, Kondo A, Nureki O, Tomita M, Aburatani H, Yachie N.
Base editors for simultaneous introduction of C-to-T and A-to-G mutations.
Nature Biotechnology. 2020 Jul;38(7):865-869. Epub 2020 Jun 2.
These authors equally contributed to this work.

Mori H, Evans-Yamamoto D, Ishiguro S, Tomita M, Yachie N.
Fast and global detection of periodic sequence repeats in large genomic resources.
Nucleic Acids Research. 2019 Jan 25;47(2):e8.

Preprints


Peer-reviewed articles

Review articles (in Japanese)

Ph.D. thesis

Books

Talks

Poster presentations

Fellowships

Software tools

QUEEN is a framework to generate quinable and efficiently editable nucleotide sequence resources to resolve many current issues in building DNA. QUEEN enables to design a new DNA by using existing DNA resource files and records the construction process in an output file (GenBank file format). The GenBank files generated by QUEEN are able to regenerate the process codes that perfectly clone themselves and bequeath the design history to successive DNA constructs that recycle their partial resources. QUEEN-generated GenBank files are compatible with the existing DNA repository services and software.

Related articles:
Mori H, Yachie N. A framework to efficiently describe and share reproducible DNA materials and construction protocols. Nat Commun. 2022 May 24;13(1):2894. doi: 10.1038/s41467-022-30588-x. 

SPADE is a software tool to explore various periodic repeat regions from large genomic and protein data resources in a high-throughput and unsupervised manner.

Related articles:

Mori H, Evans-Yamamoto D, Ishiguro S, Tomita M, Yachie N. Fast and global detection of periodic sequence repeats in large genomic resources. Nucleic Acids Res. 2019 Jan 25;47(2):e8.

Patchworklib is a universal composer of matplotlib-related plots (simple matplotlib plots, Seaborn plots (both axis-level and figure-level), and plotnine plots). This library is inspired by patchwork for ggplot2. As original patchwork, users can easily align matplotlib-related plots with only "/" and "|" operators. 

Circos plots in matplotlib

sangerseq_viewer is a python package to automatically visualize Sanger sequencing results and the corresponding annotated sequence map.