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Thomas P. Brutnell

dblp:140/3135 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2014
0000-0002-3581-8211ORCID · reported

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
model-based clustering
0.212014
Model-based clustering for RNA-seq data · Bioinform. 2014
Bioinformatics and computational biology › transcriptomics
RNA-seq analysis
0.212014
Model-based clustering for RNA-seq data · Bioinform. 2014
Bioinformatics and computational biology
transcriptomics
0.212014
Model-based clustering for RNA-seq data · Bioinform. 2014
Bioinformatics and computational biology › gene expression analysis
gene clustering
0.112014
Model-based clustering for RNA-seq data · Bioinform. 2014
Bioinformatics and computational biology
gene expression analysis
0.112014
Model-based clustering for RNA-seq data · Bioinform. 2014

Methods — techniques the papers use, named apart from their topics

hierarchical clustering · 0.2expectation-maximization · 0.2
YearPublicationVenuePosition
2014 Model-based clustering for RNA-seq data
abstract
MOTIVATION: RNA-seq technology has been widely adopted as an attractive alternative to microarray-based methods to study global gene expression. However, robust statistical tools to analyze these complex datasets are still lacking. By grouping genes with similar expression profiles across treatments, cluster analysis provides insight into gene functions and networks, and hence is an important technique for RNA-seq data analysis. RESULTS: In this manuscript, we derive clustering algorithms based on appropriate probability models for RNA-seq data. An expectation-maximization algorithm and another two stochastic versions of expectation-maximization algorithms are described. In addition, a strategy for initialization based on likelihood is proposed to improve the clustering algorithms. Moreover, we present a model-based hybrid-hierarchical clustering method to generate a tree structure that allows visualization of relationships among clusters as well as flexibility of choosing the number of clusters. Results from both simulation studies and analysis of a maize RNA-seq dataset show that our proposed methods provide better clustering results than alternative methods such as the K-means algorithm and hierarchical clustering methods that are not based on probability models. AVAILABILITY AND IMPLEMENTATION: An R package, MBCluster.Seq, has been developed to implement our proposed algorithms. This R package provides fast computation and is publicly available at http://www.r-project.org
Yaqing Si, Peng Liu 0012, Pinghua Li, Thomas P. Brutnell
Bioinform.4