ArticleInternational journal of molecular sciences2026
Triclustering Model for Three-Dimensional Time-Series Gene Expression Data.
Article in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.
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.
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.
Who cites it
0 citing papers in PubMed.
No citing paper in PubMed yet.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
4 authors.
Funding
Abstract
With the rapid advancement and cost reduction in high-throughput sequencing technologies, the accumulation of large-scale, three-dimensional gene expression data has surged. Consequently, effectively reducing the dimensionality of these complex datasets to extract critical biological information remains a significant challenge. Although various methods for identifying gene expression modules have been developed, most do not explicitly account for the multifactorial interactions among the temporal, spatial, and environmental dimensions. To address this limitation, we propose a novel three-dimensional triclustering technique based on a multivariate Gaussian mixture model (MVGMM) within a maximum likelihood framework. Specifically, our approach incorporates Legendre polynomials to model the temporal dynamics of gene expression and utilizes the Bayesian Information Criterion (BIC) to determine the optimal number of clusters. To further evaluate the model's robustness against the high background noise typically present in empirical datasets (such as
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.