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Jacqueline M. Hughes-Oliver

dblp:32/476 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2007
0000-0002-6464-9955ORCID · verified

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 2 heaviest of 2, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112007
Domain-enhanced analysis of microarray data using GO annotations · Bioinform. 2007
Bioinformatics and computational biology › protein function prediction
gene ontology annotation
0.012007
Domain-enhanced analysis of microarray data using GO annotations · Bioinform. 2007

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

top-down domain aggregation · 0.1differential expression testing · 0.1
YearPublicationVenuePosition
2007 Domain-enhanced analysis of microarray data using GO annotations
abstract
MOTIVATION: New biological systems technologies give scientists the ability to measure thousands of bio-molecules including genes, proteins, lipids and metabolites. We use domain knowledge, e.g. the Gene Ontology, to guide analysis of such data. By focusing on domain-aggregated results at, say the molecular function level, increased interpretability is available to biological scientists beyond what is possible if results are presented at the gene level. RESULTS: We use a 'top-down' approach to perform domain aggregation by first combining gene expressions before testing for differentially expressed patterns. This is in contrast to the more standard 'bottom-up' approach, where genes are first tested individually then aggregated by domain knowledge. The benefits are greater sensitivity for detecting signals. Our method, domain-enhanced analysis (DEA) is assessed and compared to other methods using simulation studies and analysis of two publicly available leukemia data sets. AVAILABILITY: Our DEA method uses functions available in R (http://www.r-project.org/) and SAS (http://www.sas.com/). The two experimental data sets used in our analysis are available in R as Bioconductor packages, 'ALL' and 'golubEsets' (http://www.bioconductor.org/). SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Jacqueline M. Hughes-Oliver, J. Alan Menius Jr.
Bioinform.2