Evidence map›Paper›PMID 29361928›Full record

ArticleBMC bioinformatics2018

Shrinkage Clustering: a fast and size-constrained clustering algorithm for biomedical applications.

Chenyue W Hu, Hanyang Li, Amina A Qutub

Abstract read
In one paragraph

Article in BMC bioinformatics, 2018. 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

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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
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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.

Chenyue W HuDepartment of Bioengineering, Rice University, Main Street, Houston, 77030, USA.
Hanyang LiDepartment of Bioengineering, Rice University, Main Street, Houston, 77030, USA.
Amina A QutubDepartment of Bioengineering, Rice University, Main Street, Houston, 77030, USA. aminaq@rice.edu.

Funding

Spatially-delineated System-level Analyses and Control of Cytoskeletal RegulationR01GM106027 · NIGMS · RICE UNIVERSITY · PI BALAZSI, GABOR, DIEHL, MICHAEL R · 2013 to 2016
$1.2M
Howard Hughes Medical InstituteNational Science Foundation CAREER 1150645NIGMS NIH HHS R01 GM106027NIH HHS R01 GM106027
6 · The paper itself

Abstract

backgroundMany common clustering algorithms require a two-step process that limits their efficiency. The algorithms need to be performed repetitively and need to be implemented together with a model selection criterion. These two steps are needed in order to determine both the number of clusters present in the data and the corresponding cluster memberships. As biomedical datasets increase in size and prevalence, there is a growing need for new methods that are more convenient to implement and are more computationally efficient. In addition, it is often essential to obtain clusters of sufficient sample size to make the clustering result meaningful and interpretable for subsequent analysis.

resultsWe introduce Shrinkage Clustering, a novel clustering algorithm based on matrix factorization that simultaneously finds the optimal number of clusters while partitioning the data. We report its performances across multiple simulated and actual datasets, and demonstrate its strength in accuracy and speed applied to subtyping cancer and brain tissues. In addition, the algorithm offers a straightforward solution to clustering with cluster size constraints.

conclusionsGiven its ease of implementation, computing efficiency and extensible structure, Shrinkage Clustering can be applied broadly to solve biomedical clustering tasks especially when dealing with large datasets.

Indexed as

AlgorithmsBrainBreast NeoplasmsCluster AnalysisDatabases, FactualFemaleGene Expression RegulationHumansNeoplasmsCancer subtypingClusteringGene expressionMatrix factorization

Identifiers

PMID29361928
PMCPMC5782397

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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.