Evidence map›Paper›PMID 35758016›Full record

ArticleDisease models & mechanisms2022

Contribution of model organism phenotypes to the computational identification of human disease genes.

Sarah M Alghamdi, Paul N Schofield, Robert Hoehndorf

Abstract read
In one paragraph

Article in Disease models & mechanisms, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Article
  3. UtilizingJournal of developmental biology · 2025
    Review
  4. Review
  5. The Use of AI for Phenotype-Genotype Mapping.Methods in molecular biology (Clifton, N.J.) · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
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.

Sarah M AlghamdiComputational Bioscience Research Center, King Abdullah University of Science and Technology, 4700 KAUST, 23955 Thuwal, Saudi Arabia.ORCID 0000-0001-5544-7166
Paul N SchofieldDepartment of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB2 3EG, UK.ORCID 0000-0002-5111-7263
Robert HoehndorfComputational Bioscience Research Center, King Abdullah University of Science and Technology, 4700 KAUST, 23955 Thuwal, Saudi Arabia.ORCID 0000-0001-8149-5890

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Computing phenotypic similarity helps identify new disease genes and diagnose rare diseases. Genotype-phenotype data from orthologous genes in model organisms can compensate for lack of human data and increase genome coverage. In the past decade, cross-species phenotype comparisons have proven valuble, and several ontologies have been developed for this purpose. The relative contribution of different model organisms to computational identification of disease-associated genes is not fully explored. We used phenotype ontologies to semantically relate phenotypes resulting from loss-of-function mutations in model organisms to disease-associated phenotypes in humans. Semantic machine learning methods were used to measure the contribution of different model organisms to the identification of known human gene-disease associations. We found that mouse genotype-phenotype data provided the most important dataset in the identification of human disease genes by semantic similarity and machine learning over phenotype ontologies. Other model organisms' data did not improve identification over that obtained using the mouse alone, and therefore did not contribute significantly to this task. Our work impacts on the development of integrated phenotype ontologies, as well as for the use of model organism phenotypes in human genetic variant interpretation. This article has an associated First Person interview with the first author of the paper.

Indexed as

Rare DiseasesSemanticsAnimalsComputational BiologyGenomeHumansMachine LearningMicePhenotypeDisease gene discoveryMachine learningModel organismOntologyPhenotypeSemantic similarity

Identifiers

PMID35758016
PMCPMC9366895

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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.