ArticleDisease models & mechanisms2025
Building a framework for reproducibility: the case for standardized data reporting and metadata integration in zebrafish research.
Article in Disease models & mechanisms, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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.
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.
Who cites it
4 citing papers in PubMed.
- Organoid Intelligent Morphomics: Decoding the organoid morphome through artificial intelligence from phenotypic quantification to mechanistic insight.Bioactive materials · 2027Review
- Potential and challenges of Positron Emission Tomography beyond conventional preclinical and clinical imaging.Zeitschrift fur medizinische Physik · 2026Review
- Neuroprotective effects of traditional Chinese medicine using zebrafish models - a review.Frontiers in pharmacology · 2026Review
- Zebrafish as a translational platform for investigating multi-organ pharmacological interactions of traditional Chinese medicine.Frontiers in pharmacology · 2026Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
Zebrafish (Danio rerio) is a leading vertebrate model that has greatly advanced research across fields such as developmental biology, toxicology, immunology and genetics. The rapid generation of high-throughput datasets fueled by advances in genomics, imaging and artificial intelligence (AI) has expanded the zebrafish as an animal model for human disease research and therapeutic discoveries. However, the absence of globally adopted, standardized data reporting methods within the zebrafish community undermines data usability, interoperability and reproducibility. Inconsistent documentation of experimental parameters - including genes, alleles, developmental stages and imaging details - creates barriers to integrating and comparing results across laboratories and disciplines. Challenges are especially pronounced for reporting developmental stages, imaging metadata and chemical exposure protocols, impeding robust data integration and reuse. Although resources such as the Zebrafish Information Network (ZFIN) and global initiatives such as the Monarch Initiative promote ontology-driven data standards, widespread implementation remains limited owing to gaps in community awareness and engagement. The use of species-specific and integrative ontologies is essential for unambiguous data annotation and reliable cross-species comparison, particularly in the context of accelerating AI-driven research. In this Editorial, we summarize current standards relevant to the zebrafish field and highlight the urgent need for collective action. Broad community participation in developing, refining and consistently adopting robust data standards will enhance reproducibility, facilitate interdisciplinary collaboration and ensure that zebrafish research remains a pillar for future scientific and AI-powered advances.
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What OpenQuestion holds
Registered trials
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.