Evidence map›Paper›PMID 41388108›Full record

ReviewNature methods2026

Computational strategies for cross-species knowledge transfer.

Hao Yuan, Christopher A Mancuso, Kayla Johnson, Ingo Braasch, Arjun Krishnan

Abstract readReview
In one paragraph

Review in Nature methods, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Review
  2. Review
  3. SPACE: STRING proteins as complementary embeddings.Bioinformatics (Oxford, England) · 2025
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

5 authors.

Hao YuanGenetics and Genome Sciences Program, Michigan State University, East Lansing, MI, USA.ORCID http://orcid.org/0000-0002-8848-1595
Christopher A MancusoDepartment of Biostatistics and Informatics, University of Colorado Anschutz, Aurora, CO, USA.ORCID http://orcid.org/0000-0003-3081-2758
Kayla JohnsonDepartment of Biomedical Informatics, University of Colorado Anschutz, Aurora, CO, USA.ORCID http://orcid.org/0000-0002-0889-5705
Ingo BraaschGenetics and Genome Sciences Program, Michigan State University, East Lansing, MI, USA. braasch@msu.edu.ORCID http://orcid.org/0000-0003-4766-611X
Arjun KrishnanDepartment of Biomedical Informatics, University of Colorado Anschutz, Aurora, CO, USA. arjun.krishnan@cuanschutz.edu.ORCID http://orcid.org/0000-0002-7980-4110

Funding

Resources for Teleost Gene Duplicates and Human DiseaseR01OD011116 · OD · UNIVERSITY OF OREGON · PI POSTLETHWAIT, JOHN H. · 2012 to 2020
$5.4M
Resolving and understanding the genomic basis of heterogeneous complex traits and diseasesR35GM128765 · NIGMS · UNIVERSITY OF COLORADO DENVER · PI KRISHNAN, ARJUN · 2018 to 2022
$2.0M
NIGMS NIH HHS R35 GM128765NIH HHS R01 OD011116ODCDC CDC HHS R01 OD011116Simons Foundation 1017799U.S. Department of Health & Human Services | NIH | NIH Office of the Director (OD) R01OD011116
6 · The paper itself

Abstract

Research organisms provide invaluable insights into human biology and diseases, serving as essential tools for functional experiments, disease modeling and drug testing. However, evolutionary divergence between humans and research organisms hinders effective knowledge transfer across species. Here, we review state-of-the-art methods for computationally transferring knowledge across species, primarily focusing on methods that use transcriptome data and/or molecular networks. Our Perspective addresses four key areas: (1) transferring disease and gene annotation knowledge across species, (2) identifying functionally equivalent molecular components, (3) inferring equivalent perturbed genes or gene sets and (4) identifying equivalent cell types. We conclude with an outlook on future directions and several key challenges that remain in cross-species knowledge transfer, including introducing the concept of 'agnology' to describe functional equivalence of biological entities, regardless of their evolutionary origins. This concept is becoming pervasive in integrative data-driven models in which evolutionary origins of functions can remain unresolved.

Indexed as

Computational BiologyAnimalsGene Regulatory NetworksHumansMolecular Sequence AnnotationSpecies SpecificityTranscriptome

Identifiers

PMID41388108
PMCPMC12970299

What OpenQuestion holds

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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.