Evidence map›Paper›PMID 42818971›Full record

ArticlebioRxiv : the preprint server for biology2026

PHAROS: turning single-cell perturbation models into target-directed drug-combination screens.

Jon Bezney, Carlo Ruggeri, Federico Borra, Lei S Qi, Francesca Buffa, Lars M Steinmetz

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Jon BezneyDepartment of Genetics, Stanford University School of Medicine, Stanford, USA.
Carlo RuggeriDepartment of Computing Sciences, Bocconi Institute for Data Science and Analytics, Milan, Italy.
Federico BorraDepartment of Computing Sciences, Bocconi Institute for Data Science and Analytics, Milan, Italy.
Lei S QiDepartment of Bioengineering, Stanford University, Stanford, USA.
Francesca BuffaDepartment of Computing Sciences, Bocconi Institute for Data Science and Analytics, Milan, Italy.ORCID 0000-0003-0409-406X
Lars M SteinmetzDepartment of Genetics, Stanford University School of Medicine, Stanford, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Combination therapies are central to cancer treatment, but exhaustive screening is impractical. We introduce PHAROS, a framework that turns a pretrained single-cell perturbation model into a target-directed search engine for drug combinations. PHAROS predicts how a cell population changes under a drug, one drug at a time, then chains these predictions together to simulate drug combinations. It scores each simulated outcome against the desired target state and uses a search algorithm to find the most promising combinations, all without retraining the underlying model. Across two independent combinatorial perturbation datasets, PHAROS recovered exact or mechanism-matched two-drug responses in cell lines, both seen and unseen during model training. Its rankings were specific to the requested conversion and were not explained by single-drug effects, additive effects, or shared mechanism of action. In exploratory analyses of patient-derived metastatic HR+/HER2

Identifiers

PMID42818971
PMCPMC13622985

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.