Evidence map›Paper›PMID 42177640›Full record

ArticleBriefings in bioinformatics2026

A scalable, multi-resolution consensus clustering approach for prioritizing robust signals from high-throughput screens.

Shaine Chenxin Bao, Kathleen I Pishas, Karla J Cowley, Qiongyi Zhao, Emily C A Goodall, Ian R Henderson, Xin Liu, Evanny Marinovic, Mark S Carey, Ian G Campbell and 4 more

Abstract read
In one paragraph

Article in Briefings in bioinformatics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

14 authors.

Shaine Chenxin BaoInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.ORCID 0009-0008-2085-8326
Kathleen I PishasPeter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Karla J CowleyVictorian Centre for Functional Genomics, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Qiongyi ZhaoInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-6341-0416
Emily C A GoodallInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.
Ian R HendersonInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.
Xin LiuPeter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Evanny MarinovicPeter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Mark S CareyDivision of Gynecology Oncology, Department of Obstetrics and Gynecology, University of British Columbia, 2775 Laurel St, Vancouver, BC, V5Z 1M9, Canada.
Ian G CampbellPeter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Kaylene J SimpsonVictorian Centre for Functional Genomics, Peter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.
Dane CheasleyPeter MacCallum Cancer Centre, 305 Grattan Street, Melbourne, VIC, 3000, Australia.ORCID 0000-0002-1170-4690
Dalia MizikovskyInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.
Nathan J PalpantInstitute for Molecular Bioscience, The University of Queensland, 306 Carmody Road, St Lucia, Brisbane, QLD, 4072, Australia.ORCID 0000-0002-9334-8107

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Modern biology increasingly relies on large-scale screening to generate high dimensional datasets with potential to accelerate discovery. However, analysing these complex datasets remains challenging, due to hierarchical biological structure, uncertainty in the true number of groups, and high dimensional noise that confounds genuine biological signal. Here we present an unsupervised consensus clustering tool, Untangled, that aggregates clustering solutions across granularities to construct a stability-based representation, followed by cluster number optimization and systematic evaluation of cluster robustness. Through extensive benchmarking on simulated datasets, ground truth datasets and diverse high-dimensional screening applications, we demonstrate that Untangled reliably recovers underlying relationships, resolves stable meaningful substructure, and more effectively prioritizes robust clusters with shared biological mechanisms and conserved phenotypic responses than alternative clustering approaches. These results establish Untangled as a scalable framework for cluster discovery to guide efficient follow-up investigation from high-dimensional biological datasets.

Indexed as

Computational BiologyHigh-Throughput Screening AssaysAlgorithmsCluster AnalysisClustering AlgorithmsHumanscomputational biologyconsensus clusteringdrug discoveryhigh dimensional data analysishigh-throughput screeningunsupervised learning

Identifiers

PMID42177640
PMCPMC13198723

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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.