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

Hidetoshi Shimokawa

dblp:220/7004 · DBLP profile ↗
← Back
3ranked-venue papers
2as first author
1since 2021 · last 2023
—ORCID · none

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

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-authorArtificial intelligence and machine learning · 1 · 1 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
1 paper
Bioinformatics and computational biology · 100%
Databases, data mining, and information retrieval
1 paper
Information retrieval · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › protein-protein interaction prediction
antibody-antigen interaction prediction
0.712023
AVIDa-hIL6: A Large-Scale VHH Dataset Produced from an Immunized Alpaca for Predicting Antigen-Antibody Interactions · NeurIPS 2023
Bioinformatics and computational biology
immunoinformatics
0.712023
AVIDa-hIL6: A Large-Scale VHH Dataset Produced from an Immunized Alpaca for Predicting Antigen-Antibody Interactions · NeurIPS 2023
Information retrieval › evaluation › benchmark dataset
benchmark dataset construction
0.712023
AVIDa-hIL6: A Large-Scale VHH Dataset Produced from an Immunized Alpaca for Predicting Antigen-Antibody Interactions · NeurIPS 2023

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

machine learning models · 1.3
YearPublicationVenuePosition
2023 AVIDa-hIL6: A Large-Scale VHH Dataset Produced from an Immunized Alpaca for Predicting Antigen-Antibody Interactions
abstract
Antibodies have become an important class of therapeutic agents to treat human diseases.To accelerate therapeutic antibody discovery, computational methods, especially machine learning, have attracted considerable interest for predicting specific interactions between antibody candidates and target antigens such as viruses and bacteria.However, the publicly available datasets in existing works have notable limitations, such as small sizes and the lack of non-binding samples and exact amino acid sequences.To overcome these limitations, we have developed AVIDa-hIL6, a large-scale dataset for predicting antigen-antibody interactions in the variable domain of heavy chain of heavy chain antibodies (VHHs), produced from an alpaca immunized with the human interleukin-6 (IL-6) protein, as antigens.By leveraging the simple structure of VHHs, which facilitates identification of full-length amino acid sequences by DNA sequencing technology, AVIDa-hIL6 contains 573,891 antigen-VHH pairs with amino acid sequences.All the antigen-VHH pairs have reliable labels for binding or non-binding, as generated by a novel labeling method.Furthermore, via introduction of artificial mutations, AVIDa-hIL6 contains 30 different mutants in addition to wild-type IL-6 protein.This characteristic provides opportunities to develop machine learning models for predicting changes in antibody binding by antigen mutations.We report experimental benchmark results on AVIDa-hIL6 by using machine learning models.The results indicate that the existing models have potential, but further research is needed to generalize them to predict effective antibodies against unknown mutants.The dataset is available at https://avida-hil6.cognanous.com.
Hirofumi Tsuruta, Hiroyuki Yamazaki, Ryota Maeda, Ryotaro Tamura, Jennifer N. Wei, Zelda Mariet, Poomarin Phloyphisut, Hidetoshi Shimokawa, Joseph R. Ledsam, Lucy J. Colwell, Akihiro Imura
NeurIPS8
2007 A Bound of Generalized Cutoff Rate for the Fixed-Length Lossy Coding of General Sources
abstract
This paper investigate Csiszar's generalized cutoff rate for the fixed-length lossy coding of general sources. We obtain an upper bound of generalized cutoff rate and derive Renyi's entropy for the case of loss-less coding. We also derive generalized cutoff rate for memory-less sources with lossy coding. It can be considered as a lossy counterpart of Renyi's entropy.
Hidetoshi Shimokawa
ISIT1
2006 Rényi's Entropy and Error Exponent of Source Coding with Countably Infinite Alphabet
abstract
This paper discuss the relation between Renyi's entropy rate and error exponent of source coding. This is a generalization of Csiszar's beta-cutoff rate. We extend the result to arbitrary discrete sources even when the alphabet is countably infinite
Hidetoshi Shimokawa
ISIT1