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James W. Miskin

dblp:09/1643 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2002
—ORCID · none

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 · 75% Medical and health informatics · 25%

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
cancer genomics
0.012002
A decomposition model to track gene expression signatures: preview on observer-independent classification of ovarian cancer · Bioinform. 2002
Bioinformatics and computational biology
gene expression analysis
0.012002
A decomposition model to track gene expression signatures: preview on observer-independent classification of ovarian cancer · Bioinform. 2002
Bioinformatics and computational biology › gene expression analysis
independent component analysis
0.012002
A decomposition model to track gene expression signatures: preview on observer-independent classification of ovarian cancer · Bioinform. 2002
Medical and health informatics › oncology
ovarian cancer classification
0.012002
A decomposition model to track gene expression signatures: preview on observer-independent classification of ovarian cancer · Bioinform. 2002

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

variational independent component analysis · 0.0
YearPublicationVenuePosition
2002 A decomposition model to track gene expression signatures: preview on observer-independent classification of ovarian cancer
abstract
Abstract Motivation: A number of algorithms and analytical models have been employed to reduce the multidimensional complexity of DNA array data and attempt to extract some meaningful interpretation of the results. These include clustering, principal components analysis, self-organizing maps, and support vector machine analysis. Each method assumes an implicit model for the data, many of which separate genes into distinct clusters defined by similar expression profiles in the samples tested. A point of concern is that many genes may be involved in a number of distinct behaviours, and should therefore be modelled to fit into as many separate clusters as detected in the multidimensional gene expression space. The analysis of gene expression data using a decomposition model that is independent of the observer involved would be highly beneficial to improve standard and reproducible classification of clinical and research samples. Results: We present a variational independent component analysis (ICA) method for reducing high dimensional DNA array data to a smaller set of latent variables, each associated with a gene signature. We present the results of applying the method to data from an ovarian cancer study, revealing a number of tissue type-specific and tissue type-independent gene signatures present in varying amounts among the samples surveyed. The observer independent results of such molecular analysis of biological samples could help identify patients who would benefit from different treatment strategies. We further explore the application of the model to similar high-throughput studies. Availability: Supporting details of the decomposition model can be found at http://www.inference.phy.cam.ac.uk/mackay/abstracts/icagenes.html and the ovarian cancer study data can be found at http://www.path.cam.ac.uk/~angio/publications/martoglioetal2002/ovcaica.html. Contact: [email protected]; [email protected] * To whom correspondence should be addressed. † These authors contributed equally to this work.
Ann-Marie Martoglio, James W. Miskin, Stephen K. Smith, David J. C. MacKay
Bioinform.2