Evidence map›Paper›PMID 41423796›Full record

ArticleBioinformatics (Oxford, England)2026

RISK: a next-generation tool for biological network annotation and visualization.

Ira Horecka, Hannes Röst

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Ira HoreckaTerrence Donnelly Centre for Cellular & Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.ORCID 0009-0001-3087-7087
Hannes RöstTerrence Donnelly Centre for Cellular & Biomolecular Research, University of Toronto, Toronto, ON M5S 3E1, Canada.ORCID 0000-0003-0990-7488

Funding

Canada Research Chairs program CRC-2022-00215CIHR 497277
6 · The paper itself

Abstract

summaryAnalyzing biological networks demands scalable annotation tools, yet existing methods fall short in clustering power, statistical flexibility, and broad data compatibility. We introduce Regional Inference of Significant Kinships (RISK), a next-generation tool that overcomes these challenges by integrating community detection algorithms, rigorous overrepresentation analysis, and a modular architecture that supports diverse network types. RISK identifies biologically coherent relationships within networks and generates publication-ready visualizations, as demonstrated by its ability to resolve compact functional modules in Saccharomyces cerevisiae protein-protein interaction and genetic interaction networks. Its application to a high-energy physics citation network reveals structured relationships among research subfields, highlighting its versatility beyond biological systems. As biological and interdisciplinary networks increase in size and complexity, RISK's scalability and adaptability make it a powerful solution for modern network analysis. AVAILABILITY AND IMPLEMENTATION: RISK is compatible with Python 3.8 or later, supports all major operating systems, and can be installed via pip. The software is open source under the GPLv3 license on GitHub (https://github.com/riskportal/risk) and archived on Zenodo (https://doi.org/10.5281/zenodo.17257418). Documentation and a step-by-step Jupyter notebook tutorial are available at https://github.com/riskportal/risk-docs.

Indexed as

Computational BiologyGene Regulatory NetworksSoftwareAlgorithmsProtein Interaction MappingProtein Interaction MapsSaccharomyces cerevisiae

Identifiers

PMID41423796
PMCPMC12766918

What OpenQuestion holds

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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.