Evidence map›Paper›PMID 39737568›Full record

ArticleBriefings in bioinformatics2024

A comprehensive benchmark study of methods for identifying significantly perturbed subnetworks in cancer.

Le Yang, Runpu Chen, Steve Goodison, Yijun Sun

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2024. 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. A Framework for Benchmarking Pathway Reconstruction Algorithms.bioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. 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

4 authors.

Le YangDepartment of Microbiology and Immunology, University at Buffalo, The State University of New York, 955 Main Street, Buffalo, New York, NY 14203, United States.
Runpu ChenDepartment of Microbiology and Immunology, University at Buffalo, The State University of New York, 955 Main Street, Buffalo, New York, NY 14203, United States.
Steve GoodisonDepartment of Quantitative Health Sciences, Mayo Clinic, 4500 San Pablo Rd S, Jacksonville, FL 32224, United States.
Yijun SunDepartment of Microbiology and Immunology, University at Buffalo, The State University of New York, 955 Main Street, Buffalo, New York, NY 14203, United States.

Funding

Prognostic analysis and progression modeling of basal-like breast cancer using multi-region sequencingR01CA269075 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI Steve Goodison, Yijun Sun · 2023 to 2026
$2.5M
Disease Progression Modeling of Bladder CancerR01CA266113 · NCI · MAYO CLINIC JACKSONVILLE · PI Steve Goodison, Yijun Sun · 2022 to 2026
$2.0M
Advanced Computational Approaches to Delineating Dynamic Cancer Progression Processes by Using Massive Static Sample DataR01CA241123 · NCI · STATE UNIVERSITY OF NEW YORK AT BUFFALO · PI GOODISON, STEVE, SUN, YIJUN · 2020 to 2024
$1.8M
NCI NIH HHS R01 CA241123NCI NIH HHS R01 CA266113NCI NIH HHS R01 CA269075
6 · The paper itself

Abstract

Network-based methods utilize protein-protein interaction information to identify significantly perturbed subnetworks in cancer and to propose key molecular pathways. Numerous methods have been developed, but to date, a rigorous benchmark analysis to compare the performance of existing approaches is lacking. In this paper, we proposed a novel benchmarking framework using synthetic data and conducted a comprehensive analysis to investigate the ability of existing methods to detect target genes and subnetworks and to control false positives, and how they perform in the presence of topological biases at both gene and subnetwork levels. Our analysis revealed insights into algorithmic performance that were previously unattainable. Based on the results of the benchmark study, we presented a practical guide for users on how to select appropriate detection methods and protein-protein interaction networks for cancer pathway identification, and provided suggestions for future algorithm development.

Indexed as

AlgorithmsBenchmarkingNeoplasmsComputational BiologyGene Regulatory NetworksHumansProtein Interaction MappingProtein Interaction Mapsbenchmark studycancer pathwaycaner driver gene identificationperturbed subnetworksprotein–protein interaction

Identifiers

PMID39737568
PMCPMC11684898

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.