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Ming-Han Chloe Tsai

dblp:388/3529 · DBLP profile ↗
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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

TopicWeightPapersLastEvidence papers
Machine learning › Reinforcement learning
multi-agent reinforcement learning
0.912025
ADIOS: Antibody Development via Opponent Shaping · ICML 2025
Machine learning › Reinforcement learning › multi-agent reinforcement learning
opponent shaping
0.912025
ADIOS: Antibody Development via Opponent Shaping · ICML 2025
Bioinformatics and computational biology
immunoinformatics
0.912025
ADIOS: Antibody Development via Opponent Shaping · ICML 2025
Bioinformatics and computational biology › protein design
therapeutic antibody design
0.912025
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
YearPublicationVenuePosition
2025 ADIOS: Antibody Development via Opponent Shaping
abstract
Anti-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
ICML6