EDBT 2026 Demo / reviewers in the wild / expert
Takamasa Kudo
dblp:215/4530
· DBLP profile ↗
2ranked-venue papers
0as first author
1since 2021 · last 2024
0000-0002-9709-5549ORCID · corroborated
Domains — the database's venue-derived domains; a paper can count in several
Applied, interdisciplinary, general and emerging computing · 2 · 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% | |
| Theoretical computer science
1 paper |
Mathematical optimization · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › functional genomics
perturbation screens |
0.8 | 1 | 2024 | Sequential Optimal Experimental Design of Perturbation Screens Guided by Multi-modal Priors · RECOMB 2024 |
Mathematical optimization › experimental design
optimal experimental design |
0.8 | 1 | 2024 | Sequential Optimal Experimental Design of Perturbation Screens Guided by Multi-modal Priors · RECOMB 2024 |
Methods — techniques the papers use, named apart from their topics
sequential optimal experimental design · 1.5multi-modal priors · 1.5
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2024 | Sequential Optimal Experimental Design of Perturbation Screens Guided by Multi-modal Priors
Romain Lopez, Jan-Christian Hütter, Takamasa Kudo, Antonio Rios, Aviv Regev |
RECOMB | 4 |
| 2016 | Deep Learning Automates the Quantitative Analysis of Individual Cells in Live-Cell Imaging ExperimentsabstractLive-cell imaging has opened an exciting window into the role cellular heterogeneity plays in dynamic, living systems. A major critical challenge for this class of experiments is the problem of image segmentation, or determining which parts of a microscope image correspond to which individual cells. Current approaches require many hours of manual curation and depend on approaches that are difficult to share between labs. They are also unable to robustly segment the cytoplasms of mammalian cells. Here, we show that deep convolutional neural networks, a supervised machine learning method, can solve this challenge for multiple cell types across the domains of life. We demonstrate that this approach can robustly segment fluorescent images of cell nuclei as well as phase images of the cytoplasms of individual bacterial and mammalian cells from phase contrast images without the need for a fluorescent cytoplasmic marker. These networks also enable the simultaneous segmentation and identification of different mammalian cell types grown in co-culture. A quantitative comparison with prior methods demonstrates that convolutional neural networks have improved accuracy and lead to a significant reduction in curation time. We relay our experience in designing and optimizing deep convolutional neural networks for this task and outline several design rules that we found led to robust performance. We conclude that deep convolutional neural networks are an accurate method that require less curation time, are generalizable to a multiplicity of cell types, from bacteria to mammalian cells, and expand live-cell imaging capabilities to include multi-cell type systems. David A. Van Valen, Takamasa Kudo, Keara M. Lane, Derek N. Macklin, Nicolas T. Quach, Mialy M. DeFelice, Inbal Maayan, Yu Tanouchi, Euan A. Ashley, Markus W. Covert |
PLoS Comput. Biol. | 2 |