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E. Papouli

dblp:39/7063 · DBLP profile ↗
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1ranked-venue papers
0as first author
0since 2021 · last 2009
—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 › biological network › network biology › network inference
gene regulatory network inference
0.112009
rHVDM: an R package to predict the activity and targets of a transcription factor · Bioinform. 2009
Bioinformatics and computational biology › gene regulation › transcription factor analysis
transcription factor target prediction
0.112009
rHVDM: an R package to predict the activity and targets of a transcription factor · Bioinform. 2009
Bioinformatics and computational biology › gene expression analysis
time course gene expression analysis
0.012009
rHVDM: an R package to predict the activity and targets of a transcription factor · Bioinform. 2009

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

optimization · 0.1dynamic mechanistic modeling · 0.1differential equation integration · 0.1
YearPublicationVenuePosition
2009 rHVDM: an R package to predict the activity and targets of a transcription factor
abstract
SUMMARY: Highly parallel genomic platforms like microarrays often present researchers with long lists of differentially expressed genes but contain little or no information on how these genes are regulated. rHVDM is a novel R package which uses gene expression time course data to predict the activity and targets of a transcription factor. In the first step, rHVDM uses a small number of known targets to derive the activity profile of a given transcription factor. Then, in a subsequent step, this activity profile is used to predict other putative targets of that transcription factor. A dynamic and mechanistic model of gene expression is at the heart of the technique. Measurement error is taken into account during the process, which allows an objective assessment of the robustness of fit and, therefore, the quality of the predictions. The package relies on efficient algorithms and vectorization to accomplish potentially time consuming tasks including optimization and differential equation integration. We demonstrate the efficiency and accuracy of rHVDM by examining the activity of the tumour-suppressing transcription factor, p53. AVAILABILITY: The version of the package presented here (1.8.1) is freely available from the Bioconductor Web site (http://bioconductor.org/packages/2.3/bioc/html/rHVDM.html).
Martino Barenco, E. Papouli, Sonia H. Shah, Daniel Brewer, Crispin J. Miller, Michael Hubank
Bioinform.2