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Carmen D. Tekwe

dblp:117/4154 · DBLP profile ↗
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1ranked-venue papers
1as first author
0since 2021 · last 2012
0000-0002-1857-2416ORCID · reported

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

Applied, interdisciplinary, general and emerging computing · 1 · 1 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 3 heaviest of 3, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › proteomics › proteome comparison
differential protein expression analysis
0.112012
Application of survival analysis methodology to the quantitative analysis of LC-MS proteomics data · Bioinform. 2012
Bioinformatics and computational biology
proteomics
0.112012
Application of survival analysis methodology to the quantitative analysis of LC-MS proteomics data · Bioinform. 2012
Bioinformatics and computational biology › biostatistics
statistical methods for omics data
0.112012
Application of survival analysis methodology to the quantitative analysis of LC-MS proteomics data · Bioinform. 2012

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

wilcoxon-mann-whitney test · 0.1kolmogorov-smirnov test · 0.1accelerated failure time model · 0.1
YearPublicationVenuePosition
2012 Application of survival analysis methodology to the quantitative analysis of LC-MS proteomics data
abstract
MOTIVATION: Protein abundance in quantitative proteomics is often based on observed spectral features derived from liquid chromatography mass spectrometry (LC-MS) or LC-MS/MS experiments. Peak intensities are largely non-normal in distribution. Furthermore, LC-MS-based proteomics data frequently have large proportions of missing peak intensities due to censoring mechanisms on low-abundance spectral features. Recognizing that the observed peak intensities detected with the LC-MS method are all positive, skewed and often left-censored, we propose using survival methodology to carry out differential expression analysis of proteins. Various standard statistical techniques including non-parametric tests such as the Kolmogorov-Smirnov and Wilcoxon-Mann-Whitney rank sum tests, and the parametric survival model and accelerated failure time-model with log-normal, log-logistic and Weibull distributions were used to detect any differentially expressed proteins. The statistical operating characteristics of each method are explored using both real and simulated datasets. RESULTS: Survival methods generally have greater statistical power than standard differential expression methods when the proportion of missing protein level data is 5% or more. In particular, the AFT models we consider consistently achieve greater statistical power than standard testing procedures, with the discrepancy widening with increasing missingness in the proportions. AVAILABILITY: The testing procedures discussed in this article can all be performed using readily available software such as R. The R codes are provided as supplemental materials. CONTACT: [email protected].
Carmen D. Tekwe, Raymond J. Carroll, Alan R. Dabney
Bioinform.1