Evidence map›Paper›PMID 40501811›Full record

ArticlebioRxiv : the preprint server for biology2025

A conditional generative model to disentangle morphological variation from batch effects in model organism imaging studies.

Ricardo M Valdarrago, Hongru Hu, Ruoxin Li, José Miguel Uribe-Salazar, Megan Y Dennis, 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

6 authors.

Ricardo M ValdarragoDepartment of Molecular and Cellular Biology, University of California, Davis, CA, USA.
Hongru HuDepartment of Molecular and Cellular Biology, University of California, Davis, CA, USA.
Ruoxin LiDepartment of Molecular and Cellular Biology, University of California, Davis, CA, USA.
José Miguel Uribe-SalazarGenome Center, University of California, Davis, CA, USA.
Megan Y DennisGenome Center, University of California, Davis, CA, USA.
Gerald QuonDepartment of Molecular and Cellular Biology, University of California, Davis, CA, USA.ORCID 0000-0002-1716-0153

Funding

Research Project: Pathologic Significance of Maternal AutoantibodiesP50HD103526 · NICHD · UNIVERSITY OF CALIFORNIA AT DAVIS · PI JUDY A. VAN DE WATER · 2020 to 2026
$9.7M
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
Human gene duplications in neurodevelopment and diseaseR01MH132818 · NIMH · UNIVERSITY OF CALIFORNIA AT DAVIS · PI DENNIS, MEGAN Y · 2023 to 2024
$1.4M
NICHD NIH HHS P50 HD103526NIMH NIH HHS DP2 MH129987NIMH NIH HHS R01 MH132818
6 · The paper itself

Abstract

Identifying organism-level phenotypic variation that arises from genetic variation is a longstanding problem in genetics. Model organisms such as zebrafish are frequently used for genotype to phenotype studies as they can be genetically manipulated, grown and phenotyped for morphological changes in a high throughput manner through automated systems and imaging. However, individuals from model organisms are typically grown in groups: clutches for zebrafish and frogs, and litter for rodents. These clutches act as strong confounders during image analysis, as individuals from different genotypes but grown in the same clutch tend to look more similar to each other than to individuals with the same genotype in other clutches. Existing approaches such as conditional image classification models and domain adaptation approaches perform poorly on addressing these technical batch effects. Here, we propose a conditional latent diffusion model (cLDM) that disentangles these technical batch effects from morphological features by explicitly conditioning on batch-specific variables during generation, enabling targeted separation of technical artifacts from biologically relevant data. This approach enables accurate classification of genotypes using morphological images of individual zebrafish from distinct mutant classes. Furthermore, this approach allows us to efficiently correct for batch effect and demonstrates the versatility of cLDM in tackling domain-specific problems. This work highlights the potential of cLDM to overcome batch effects and extract meaningful features.

Identifiers

PMID40501811
PMCPMC12157389

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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.