EDBT 2026 Demo / reviewers in the wild / expert
Ming-Han Chloe Tsai
dblp:388/3529
· DBLP profile ↗
1ranked-venue papers
0as first author
1since 2021 · last 2025
—ORCID · none
Domains — the database's venue-derived domains; a paper can count in several
Artificial 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.
| Artificial intelligence
1 paper |
Reinforcement learning · 100% | |
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 4 heaviest of 4, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Reinforcement learning
multi-agent reinforcement learning |
0.9 | 1 | 2025 | ADIOS: Antibody Development via Opponent Shaping · ICML 2025 |
Machine learning › Reinforcement learning › multi-agent reinforcement learning
opponent shaping |
0.9 | 1 | 2025 | ADIOS: Antibody Development via Opponent Shaping · ICML 2025 |
Bioinformatics and computational biology
immunoinformatics |
0.9 | 1 | 2025 | ADIOS: Antibody Development via Opponent Shaping · ICML 2025 |
Bioinformatics and computational biology › protein design
therapeutic antibody design |
0.9 | 1 | 2025 | ADIOS: Antibody Development via Opponent Shaping · ICML 2025 |
Methods — techniques the papers use, named apart from their topics
viral evolution simulation · 1.7opponent shaping · 1.7meta-learning · 1.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | ADIOS: Antibody Development via Opponent ShapingabstractAnti-viral therapies are typically designed to target only the current strains of a virus, a myopic response. However, therapy-induced selective pressures drive the emergence of new viral strains, against which the original myopic therapies are no longer effective. This evolutionary response presents an opportunity: our therapies could both defend against and actively influence viral evolution. This motivates our method ADIOS: Antibody Development vIa Opponent Shaping. ADIOS is a meta-learning framework where the process of antibody therapy design, the outer loop, accounts for the virus’s adaptive response, the inner loop. With ADIOS, antibodies are not only robust against potential future variants, they also influence, i.e. shape, which future variants emerge. In line with the opponent shaping literature, we refer to our optimised antibodies as shapers. To demonstrate the value of ADIOS, we build a viral evolution simulator using the Absolut! framework, in which shapers successfully target both current and future viral variants, outperforming myopic antibodies. Furthermore, we show that shapers modify the distribution over viral evolutionary trajectories to result in weaker variants. We believe that our ADIOS paradigm will facilitate the discovery of long-lived vaccines and antibody therapies while also generalising to other domains. Specifically, domains such as antimicrobial resistance, cancer treatment, and others with evolutionarily adaptive opponents. Our code is available at https://github.com/olakalisz/adios. Sebastian Towers, Aleksandra Kalisz, Philippe A. Robert, Alicia Higueruelo, Francesca V. Vianello, Ming-Han Chloe Tsai, Harrison Steel, Jakob N. Foerster |
ICML | 6 |