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James C. Ford

dblp:93/6068 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2005
—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 · 100%

Topics — the 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
gene expression analysis
0.112005
HykGene: a hybrid approach for selecting marker genes for phenotype classification using microarray gene expression data · Bioinform. 2005
Bioinformatics and computational biology › gene expression analysis › gene expression classification
marker gene selection
0.112005
HykGene: a hybrid approach for selecting marker genes for phenotype classification using microarray gene expression data · Bioinform. 2005
Bioinformatics and computational biology
phenotype classification
0.112005
HykGene: a hybrid approach for selecting marker genes for phenotype classification using microarray gene expression data · Bioinform. 2005

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

sweep-line algorithm · 0.1hierarchical clustering · 0.1gene ranking · 0.1
YearPublicationVenuePosition
2005 HykGene: a hybrid approach for selecting marker genes for phenotype classification using microarray gene expression data
abstract
MOTIVATION: Recent studies have shown that microarray gene expression data are useful for phenotype classification of many diseases. A major problem in this classification is that the number of features (genes) greatly exceeds the number of instances (tissue samples). It has been shown that selecting a small set of informative genes can lead to improved classification accuracy. Many approaches have been proposed for this gene selection problem. Most of the previous gene ranking methods typically select 50-200 top-ranked genes and these genes are often highly correlated. Our goal is to select a small set of non-redundant marker genes that are most relevant for the classification task. RESULTS: To achieve this goal, we developed a novel hybrid approach that combines gene ranking and clustering analysis. In this approach, we first applied feature filtering algorithms to select a set of top-ranked genes, and then applied hierarchical clustering on these genes to generate a dendrogram. Finally, the dendrogram was analyzed by a sweep-line algorithm and marker genes are selected by collapsing dense clusters. Empirical study using three public datasets shows that our approach is capable of selecting relatively few marker genes while offering the same or better leave-one-out cross-validation accuracy compared with approaches that use top-ranked genes directly for classification. AVAILABILITY: The HykGene software is freely available at http://www.cs.dartmouth.edu/~wyh/software.htm CONTACT: [email protected] SUPPLEMENTARY INFORMATION: Supplementary material is available from http://www.cs.dartmouth.edu/~wyh/hykgene/supplement/index.htm.
Fillia Makedon, James C. Ford, Justin D. Pearlman
Bioinform.3