Demo Data from EDBT 2026 / reviewers in the wild / expert
Juan Sebastián Rodríguez Vera
dblp:393/2468
· 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 |
Deep learning architectures and training · 100% | |
| Interdisciplinary, comprehensive, and emerging computing
1 paper |
Bioinformatics and computational biology · 100% |
Topics — the 2 heaviest of 2, each with the papers that count most for it
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Machine learning › Deep learning architectures and training
foundation model |
0.9 | 1 | 2025 | ViTally Consistent: Scaling Biological Representation Learning for Cell Microscopy · ICML 2025 |
Bioinformatics and computational biology › bioimage informatics › bioimage analysis
microscopy image analysis |
0.9 | 1 | 2025 | ViTally Consistent: Scaling Biological Representation Learning for Cell Microscopy · ICML 2025 |
Methods — techniques the papers use, named apart from their topics
vision transformer · 1.7masked autoencoder · 1.7linear probing · 1.7
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2025 | ViTally Consistent: Scaling Biological Representation Learning for Cell MicroscopyabstractDeriving insights from experimentally generated datasets requires methods that can account for random and systematic measurement errors and remove them in order to accurately represent the underlying effects of the conditions being tested. Here we present a framework for pretraining on large-scale microscopy datasets that includes three steps: (1) curating a set of diverse and self-consistent training samples, (2) scaling training of an appropriate foundation model architecture on this dataset, (3) evaluating intermediate layers of the trained model to identify the best representation for downstream tasks. Using this strategy, we present the largest foundation model for cell microscopy data to our knowledge, a new 1.9 billion-parameter ViT-G/8 MAE trained on over 8 billion microscopy image crops. Compared to a previous published ViT-L/8 MAE, our new model achieves a 60% improvement in linear separability of genetic perturbations and obtains the best overall performance on whole-genome relationship recall, batch correction replicate consistency, and compound-gene activity prediction benchmarks. Kian Kenyon-Dean, Zitong Jerry Wang, John Urbanik, Konstantin Donhauser, Jason S. Hartford, Saber Saberian, Nil Sahin, Ihab Bendidi, Safiye Celik, Juan Sebastián Rodríguez Vera, Marta M. Fay, Imran S. Haque, Oren Kraus |
ICML | 10 |