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Richard E. Kennedy

dblp:68/6798 · DBLP profile ↗
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2ranked-venue papers
2as first author
0since 2021 · last 2006
0000-0003-4638-126XORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 2 · 2 first-author

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

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › gene expression analysis
differential expression analysis
0.112006
SScore: an R package for detecting differential gene expression without gene expression summaries · Bioinform. 2006
Bioinformatics and computational biology
gene expression analysis
0.112006
SScore: an R package for detecting differential gene expression without gene expression summaries · Bioinform. 2006
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112006
SScore: an R package for detecting differential gene expression without gene expression summaries · Bioinform. 2006
Bioinformatics and computational biology › gene expression analysis › microarray data preprocessing
probe-level analysis
0.112006
SScore: an R package for detecting differential gene expression without gene expression summaries · Bioinform. 2006

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

s-score algorithm · 0.1
YearPublicationVenuePosition
2006 SScore: an R package for detecting differential gene expression without gene expression summaries
abstract
SUMMARY: SScore is an R package that facilitates the comparison of gene expression between Affymetrix GeneChips using the S-score algorithm. The S-score algorithm uses probe level data directly to assess differences in gene expression, without requiring a preliminary separate step of probe set expression summary estimation. Therefore, the algorithm avoids introduction of error associated with the expression summary estimation process and has been demonstrated to improve the accuracy of identifying differentially expressed genes. The S-score produces accurate results even when few or no replicates are available. AVAILABILITY: The R package SScore is available from Bioconductor at http://www.bioconductor.org
Richard E. Kennedy, Robnet T. Kerns, Xiangrong Kong, Kellie J. Archer, Michael F. Miles
Bioinform.1
2006 Empirical validation of the S-Score algorithm in the analysis of gene expression data
abstract
BACKGROUND: Current methods of analyzing Affymetrix GeneChip microarray data require the estimation of probe set expression summaries, followed by application of statistical tests to determine which genes are differentially expressed. The S-Score algorithm described by Zhang and colleagues is an alternative method that allows tests of hypotheses directly from probe level data. It is based on an error model in which the detected signal is proportional to the probe pair signal for highly expressed genes, but approaches a background level (rather than 0) for genes with low levels of expression. This model is used to calculate relative change in probe pair intensities that converts probe signals into multiple measurements with equalized errors, which are summed over a probe set to form the S-Score. Assuming no expression differences between chips, the S-Score follows a standard normal distribution, allowing direct tests of hypotheses to be made. Using spike-in and dilution datasets, we validated the S-Score method against comparisons of gene expression utilizing the more recently developed methods RMA, dChip, and MAS5. RESULTS: The S-score showed excellent sensitivity and specificity in detecting low-level gene expression changes. Rank ordering of S-Score values more accurately reflected known fold-change values compared to other algorithms. CONCLUSION: The S-score method, utilizing probe level data directly, offers significant advantages over comparisons using only probe set expression summaries.
Richard E. Kennedy, Kellie J. Archer, Michael F. Miles
BMC Bioinform.1