A Bayesian Approach for Clustering Constant-Wise Change-Point Data

Change-point models deal with ordered data sequences. Their primary goal is to infer the locations where an aspect of the data sequence changes. In this paper, we propose and implement a nonparametric Bayesian model for clustering observations based on their constant-wise change-point profiles via a Gibbs sampler. Our model incorporates a Dirichlet process on the constant-wise change-point structures to cluster observations while simultaneously performing multiple change-point estimation. Additionally, our approach controls the number of clusters in the model, not requiring specification of the number of clusters a priori. Satisfactory clustering and estimation results were obtained when evaluating our method under various simulated scenarios and on a real dataset from single-cell genomic sequencing. Our proposed methodology is implemented as an R package called BayesCPclust and is available from the Comprehensive R Archive Network.

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Journal
Stats
Published
2026-03-17
DOI
https://doi.org/10.3390/stats9020031
Primary Topic
Bayesian Methods and Mixture Models
Type
article
Field-Weighted Citation Impact
0.00
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article

A Bayesian Approach for Clustering Constant-Wise Change-Point Data

Ana Carolina da Cruz, Camila P. E. de Souza
Stats
Bayesian Methods and Mixture Models
article

A Bayesian Approach for Clustering Constant-Wise Change-Point Data

Ana Carolina da Cruz, Camila P. E. de Souza
article en

Abstract

Change-point models deal with ordered data sequences. Their primary goal is to infer the locations where an aspect of the data sequence changes. In this paper, we propose and implement a nonparametric Bayesian model for clustering observations based on their constant-wise change-point profiles via a Gibbs sampler. Our model incorporates a Dirichlet process on the constant-wise change-point structures to cluster observations while simultaneously performing multiple change-point estimation. Additionally, our approach controls the number of clusters in the model, not requiring specification of the number of clusters a priori. Satisfactory clustering and estimation results were obtained when evaluating our method under various simulated scenarios and on a real dataset from single-cell genomic sequencing. Our proposed methodology is implemented as an R package called BayesCPclust and is available from the Comprehensive R Archive Network.

StatsVol. 9(2)
Western University (CA)
Openalex Percentile: Top 22%
Bayesian Methods and Mixture Models
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