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Hans-Hermann Wessels

dblp:336/3236 · 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.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › functional genomics
CRISPR screening
0.912025
Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations · ICML 2025
Bioinformatics and computational biology › drug discovery
drug combination prediction
0.912025
Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations · ICML 2025
Bioinformatics and computational biology
genomics
0.912025
Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations · ICML 2025

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

gene embedding · 0.9adaptive embedding · 0.9active learning · 0.9
YearPublicationVenuePosition
2025 Active Learning for Efficient Discovery of Optimal Combinatorial Perturbations
abstract
Combinatorial CRISPR screening enables large-scale identification of synergistic gene pairs for combination therapies, but exhaustive experimentation is infeasible. We introduce NAIAD, an active learning framework that efficiently discovers optimal gene pairs by leveraging single-gene perturbation effects and adaptive gene embeddings that scale with the training data size, mitigating overfitting in small-sample learning while capturing complex gene interactions as more data is collected. Evaluated on four CRISPR datasets with over 350,000 interactions, NAIAD trained on small datasets outperforms existing models by up to 40%. Its recommendation system prioritizes gene pairs with maximum predicted effects, accelerating discovery with fewer experiments. We also extend NAIAD to optimal drug combination identification among 2,000 candidates. Overall, NAIAD enhances combinatorial perturbation design and drives advances in genomics research and therapeutic development in combination therapy. Our code is publicly available at: https://github.com/NeptuneBio/NAIAD
Jason Qin, Hans-Hermann Wessels, Carlos Fernandez-Granda, Yuhan Hao
ICML2