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Satoshi Uematsu

dblp:330/4768 · DBLP profile ↗
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3ranked-venue papers
0as first author
3since 2021 · last 2023
0000-0002-5347-6737ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 3 · 3 since 2021

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 5 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › network bioinformatics
biological network analysis
0.712023
ggkegg: analysis and visualization of KEGG data utilizing the grammar of graphics · Bioinform. 2023
Bioinformatics and computational biology › systems bioinformatics › pathway analysis
pathway visualization
0.712023
ggkegg: analysis and visualization of KEGG data utilizing the grammar of graphics · Bioinform. 2023
Bioinformatics and computational biology › metagenomics
phage identification
0.612022
Identification of bacteriophage genome sequences with representation learning · Bioinform. 2022
Bioinformatics and computational biology › computational microbiology
microbiome analysis
0.212023
ggkegg: analysis and visualization of KEGG data utilizing the grammar of graphics · Bioinform. 2023
Bioinformatics and computational biology › single-cell analysis
single-cell transcriptomics
0.212023
ggkegg: analysis and visualization of KEGG data utilizing the grammar of graphics · Bioinform. 2023

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

grammar of graphics · 0.7pre-training · 0.6deep representation learning · 0.6alignment-free classification · 0.6
YearPublicationVenuePosition
2023 Zero-shot-capable identification of phage-host relationships with whole-genome sequence representation by contrastive learning
abstract
Accurately identifying phage-host relationships from their genome sequences is still challenging, especially for those phages and hosts with less homologous sequences. In this work, focusing on identifying the phage-host relationships at the species and genus level, we propose a contrastive learning based approach to learn whole-genome sequence embeddings that can take account of phage-host interactions (PHIs). Contrastive learning is used to make phages infecting the same hosts close to each other in the new representation space. Specifically, we rephrase whole-genome sequences with frequency chaos game representation (FCGR) and learn latent embeddings that 'encapsulate' phages and host relationships through contrastive learning. The contrastive learning method works well on the imbalanced dataset. Based on the learned embeddings, a proposed pipeline named CL4PHI can predict known hosts and unseen hosts in training. We compare our method with two recently proposed state-of-the-art learning-based methods on their benchmark datasets. The experiment results demonstrate that the proposed method using contrastive learning improves the prediction accuracy on known hosts and demonstrates a zero-shot prediction capability on unseen hosts. In terms of potential applications, the rapid pace of genome sequencing across different species has resulted in a vast amount of whole-genome sequencing data that require efficient computational methods for identifying phage-host interactions. The proposed approach is expected to address this need by efficiently processing whole-genome sequences of phages and prokaryotic hosts and capturing features related to phage-host relationships for genome sequence representation. This approach can be used to accelerate the discovery of phage-host interactions and aid in the development of phage-based therapies for infectious diseases.
Zeheng Bai, Kosuke Fujimoto, Satoshi Uematsu, Seiya Imoto
Briefings Bioinform.5
2023 ggkegg: analysis and visualization of KEGG data utilizing the grammar of graphics
abstract
SUMMARY: The Kyoto Encyclopedia of Genes and Genomes (KEGG) database serves as a valuable systems biology resource and is widely utilized in diverse research fields. However, existing software does not allow flexible visualization and network analyses of the vast and complex KEGG data. We developed ggkegg, an R package that integrates KEGG information with ggplot2 and ggraph. ggkegg enables enhanced visualization and network analyses of KEGG data. We demonstrate the utility of the package by providing examples of its application in single-cell, bulk transcriptome, and microbiome analyses. ggkegg may empower researchers to analyze complex biological networks and present their results effectively. AVAILABILITY AND IMPLEMENTATION: The package and user documentation are available at: https://github.com/noriakis/ggkegg.
Noriaki Sato, Miho Uematsu, Kosuke Fujimoto, Satoshi Uematsu, Seiya Imoto
Bioinform.4
2022 Identification of bacteriophage genome sequences with representation learning
abstract
MOTIVATION: Bacteriophages/phages are the viruses that infect and replicate within bacteria and archaea, and rich in human body. To investigate the relationship between phages and microbial communities, the identification of phages from metagenome sequences is the first step. Currently, there are two main methods for identifying phages: database-based (alignment-based) methods and alignment-free methods. Database-based methods typically use a large number of sequences as references; alignment-free methods usually learn the features of the sequences with machine learning and deep learning models. RESULTS: We propose INHERIT which uses a deep representation learning model to integrate both database-based and alignment-free methods, combining the strengths of both. Pre-training is used as an alternative way of acquiring knowledge representations from existing databases, while the BERT-style deep learning framework retains the advantage of alignment-free methods. We compare INHERIT with four existing methods on a third-party benchmark dataset. Our experiments show that INHERIT achieves a better performance with the F1-score of 0.9932. In addition, we find that pre-training two species separately helps the non-alignment deep learning model make more accurate predictions. AVAILABILITY AND IMPLEMENTATION: The codes of INHERIT are now available in: https://github.com/Celestial-Bai/INHERIT. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Zeheng Bai, Satoru Miyano, Rui Yamaguchi, Kosuke Fujimoto, Satoshi Uematsu, Seiya Imoto
Bioinform.6