Evidence map›Paper›PMID 40950226›Full record

ArticlebioRxiv : the preprint server for biology2025

Predicting emergent phenotypes from single cell populations using CELLECTION.

Hongru Hu, Siddhant Sanghi, Gerald Quon

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2025. 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

3 authors.

Hongru HuIntegrative Genetics and Genomics Graduate Group, University of California, Davis, CA, 95616, USA.ORCID 0000-0003-0497-4796
Siddhant SanghiIntegrative Genetics and Genomics Graduate Group, University of California, Davis, CA, 95616, USA.
Gerald QuonIntegrative Genetics and Genomics Graduate Group, University of California, Davis, CA, 95616, USA.

Funding

Linking genetics to cellular behavior and disease via multimodal data integrationDP2MH129987 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI QUON, GERALD · 2021 to 2024
$2.3M
NIMH NIH HHS DP2 MH129987
6 · The paper itself

Abstract

Biological systems exhibit emergent phenotypes that arise from the collective behavior of individual components, such as whole-organ functions that arise from the coordinated activity of its individual cells, or organism-level phenotypes that result from the functional interplay of collections of genes in the genome. We present CELLECTION, a deep learning framework that learns to associate subgroups of instances with different emergent phenotypes. We show CELLECTION enables interpretable predictions for heterogeneous tasks, including disease classification, identification of disease-associated cell subtypes, alignment of developmental stages between human model systems, and even predicting relative hand-wing indices across the avian lineage. CELLECTION therefore provides a scalable and flexible framework for identifying key cellular or genetic signatures underlying complex traits in development, disease, and evolution.

Identifiers

PMID40950226
PMCPMC12424641

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

None linked

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.