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David Peel

dblp:89/2717 · DBLP profile ↗
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4ranked-venue papers
0as first author
0since 2021 · last 2002
0000-0001-5281-2041ORCID · corroborated

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

Artificial intelligence and machine learning · 2Graphics, computer vision, multimedia, augmented reality and games · 2Applied, 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%
Artificial intelligence
1 paper
Probabilistic and Bayesian machine learning · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.012002
A mixture model-based approach to the clustering of microarray expression data · Bioinform. 2002
Bioinformatics and computational biology › gene expression analysis
model-based clustering
0.012002
A mixture model-based approach to the clustering of microarray expression data · Bioinform. 2002
Machine learning › Probabilistic and Bayesian machine learning › structured models › latent variable model
mixture model
0.012000
Mixtures of Factor Analyzers · ICML 2000
Machine learning › Probabilistic and Bayesian machine learning › structured models › latent variable model › mixture model
mixture of factor analyzers
0.012000
Mixtures of Factor Analyzers · ICML 2000

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

t distribution mixture · 0.0mixture of factor analyzers · 0.0factor analysis · 0.0EM algorithm · 0.0
YearPublicationVenuePosition
2002 A mixture model-based approach to the clustering of microarray expression data
abstract
MOTIVATION: This paper introduces the software EMMIX-GENE that has been developed for the specific purpose of a model-based approach to the clustering of microarray expression data, in particular, of tissue samples on a very large number of genes. The latter is a nonstandard problem in parametric cluster analysis because the dimension of the feature space (the number of genes) is typically much greater than the number of tissues. A feasible approach is provided by first selecting a subset of the genes relevant for the clustering of the tissue samples by fitting mixtures of t distributions to rank the genes in order of increasing size of the likelihood ratio statistic for the test of one versus two components in the mixture model. The imposition of a threshold on the likelihood ratio statistic used in conjunction with a threshold on the size of a cluster allows the selection of a relevant set of genes. However, even this reduced set of genes will usually be too large for a normal mixture model to be fitted directly to the tissues, and so the use of mixtures of factor analyzers is exploited to reduce effectively the dimension of the feature space of genes. RESULTS: The usefulness of the EMMIX-GENE approach for the clustering of tissue samples is demonstrated on two well-known data sets on colon and leukaemia tissues. For both data sets, relevant subsets of the genes are able to be selected that reveal interesting clusterings of the tissues that are either consistent with the external classification of the tissues or with background and biological knowledge of these sets. AVAILABILITY: EMMIX-GENE is available at http://www.maths.uq.edu.au/~gjm/emmix-gene/
Geoffrey J. McLachlan, Richard Bean 0001, David Peel
Bioinform.3
2000 Mixtures of Factor Analyzers
Geoffrey J. McLachlan, David Peel
ICML2
1998 MIXFIT: an algorithm for the automatic fitting and testing of normal mixture models
abstract
We consider the fitting of normal mixture models to multivariate data, using maximum likelihood via the EM algorithm. This approach requires the specification of all initial estimate of the vector of unknown parameters, or equivalently, of an initial classification of the data with respect to the components of the mixture model underfit. We describe an algorithm called MIXFIT that automatically undertakes this fitting, including the specification of suitable initial values if not supplied by the user The MIXFIT algorithm has several options, including the provision to carry out a resampling-based test for the number of components in the mixture model.
Geoffrey J. McLachlan, David Peel
ICPR2
1996 Maximum likelihood clustering via normal mixture models
Geoffrey J. McLachlan, David Peel, W. J. Whiten
Signal Process. Image Commun.2