Marvin Sextro

Marvin Sextro

@marvinsextro.de

Machine Learning for Precision Medicine PhD student at BIFOLD & TU Berlin Data Scientist at Aignostics https://marvinsextro.de

141 followers197 following9 posts

[1/3] Happy to share that our paper "MapPFN: Learning Causal Perturbation Maps in Context" has been accepted at NeurIPS 2026! 🎉 TL;DR: We frame perturbation prediction as an in-context learning problem given a set of interventional experiments.

[1/6] How can we build virtual cell foundation models that adapt to unseen biological contexts? Meet MapPFN, the first prior-data fitted network (PFN) for perturbation prediction. Meta-learned from a synthetic biological prior, it adapts at inference via in-context learning. 🧵

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[6/6] My amazing co-author Weronika Kłos will present MapPFN at the Generative AI in Genomics Workshop (Gen²) at #ICLR2026 in Rio. 🇧🇷 📅 Mon, Apr 27, 2026, 1:10–1:55 PM (UTC-3) 📍 Room 211, Riocentro Convention and Event Center

[1/6] How can we build virtual cell foundation models that adapt to unseen biological contexts? Meet MapPFN, the first prior-data fitted network (PFN) for perturbation prediction. Meta-learned from a synthetic biological prior, it adapts at inference via in-context learning. 🧵

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[3/6] MapPFN meta-learns to map pre- to post-perturbation distributions from a synthetic biological prior of in silico gene knockouts, decoupling it from limited experimental data. At inference, it adapts to unseen biological contexts via in-context learning.

[4/6] A single pre-trained MapPFN adapts to new datasets and arbitrary gene sets. Zero-shot, it recovers differentially expressed genes on par with baselines trained on real single-cell data. Fine-tuned, it consistently outperforms baselines across downstream datasets.

[1/6] How can we build virtual cell foundation models that adapt to unseen biological contexts? Meet MapPFN, the first prior-data fitted network (PFN) for perturbation prediction. Meta-learned from a synthetic biological prior, it adapts at inference via in-context learning. 🧵

[2/6] Single-cell perturbation datasets cover only a tiny slice of possible interventions and cell states. Existing methods cannot leverage new interventional evidence at inference time, forcing them to retrain for every new dataset.

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