Demonstration venue · read-only. Every page can be browsed; the buttons that would change it are switched off. Create an account to run TaxoReview on your own data. A simulation from public publication records: the people listed were not invited and did not agree to review.
? Tutorial for this page

Ikuo Fukuda

dblp:28/7929 · DBLP profile ↗
← Back
1ranked-venue papers
0as first author
0since 2021 · last 2016
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Computational science and engineering · 100%

Topics — the 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Computational science and engineering › computational chemistry › molecular simulation
molecular dynamics
0.212016
mDCC_tools: characterizing multi-modal atomic motions in molecular dynamics trajectories · Bioinform. 2016
Computational science and engineering › computational chemistry › molecular simulation › molecular dynamics
trajectory analysis
0.212016
mDCC_tools: characterizing multi-modal atomic motions in molecular dynamics trajectories · Bioinform. 2016

Methods — techniques the papers use, named apart from their topics

dynamic cross-correlation · 0.2complex network analysis · 0.2bayesian pattern recognition · 0.2
YearPublicationVenuePosition
2016 mDCC_tools: characterizing multi-modal atomic motions in molecular dynamics trajectories
abstract
UNLABELLED: We previously reported the multi-modal Dynamic Cross Correlation (mDCC) method for analyzing molecular dynamics trajectories. This method quantifies the correlation coefficients of atomic motions with complex multi-modal behaviors by using a Bayesian-based pattern recognition technique that can effectively capture transiently formed, unstable interactions. Here, we present an open source toolkit for performing the mDCC analysis, including pattern recognitions, complex network analyses and visualizations. We include a tutorial document that thoroughly explains how to apply this toolkit for an analysis, using the example trajectory of the 100 ns simulation of an engineered endothelin-1 peptide dimer. AVAILABILITY AND IMPLEMENTATION: The source code is available for free at http://www.protein.osaka-u.ac.jp/rcsfp/pi/mdcctools/, implemented in C ++ and Python, and supported on Linux. CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Kota Kasahara, Neetha Mohan, Ikuo Fukuda, Haruki Nakamura
Bioinform.3