Demo Data from EDBT 2026 / reviewers in the wild / expert
Renaud Gaujoux
dblp:06/8710
· DBLP profile ↗
2ranked-venue papers
2as first author
0since 2021 · last 2013
—ORCID · none
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
| Topic | Weight | Papers | Last | Evidence papers |
|---|---|---|---|---|
Bioinformatics and computational biology › omics data analysis
cell-type deconvolution |
0.2 | 1 | 2013 | CellMix: a comprehensive toolbox for gene expression deconvolution · Bioinform. 2013 |
Bioinformatics and computational biology
gene expression analysis |
0.2 | 1 | 2013 | CellMix: a comprehensive toolbox for gene expression deconvolution · Bioinform. 2013 |
Bioinformatics and computational biology › gene expression analysis › gene expression quantification
gene expression deconvolution |
0.2 | 1 | 2013 | CellMix: a comprehensive toolbox for gene expression deconvolution · Bioinform. 2013 |
Bioinformatics and computational biology › gene expression analysis
differential expression analysis |
0.0 | 1 | 2013 | CellMix: a comprehensive toolbox for gene expression deconvolution · Bioinform. 2013 |
Methods — techniques the papers use, named apart from their topics
regression · 0.2matrix factorization · 0.2
| Year | Publication | Venue | Position |
|---|---|---|---|
| 2013 | CellMix: a comprehensive toolbox for gene expression deconvolutionabstractUNLABELLED: Gene expression data are typically generated from heterogeneous biological samples that are composed of multiple cell or tissue types, in varying proportions, each contributing to global gene expression. This heterogeneity is a major confounder in standard analysis such as differential expression analysis, where differences in the relative proportions of the constituent cells may prevent or bias the detection of cell-specific differences. Computational deconvolution of global gene expression is an appealing alternative to costly physical sample separation techniques and enables a more detailed analysis of the underlying biological processes at the cell-type level. To facilitate and popularize the application of such methods, we developed CellMix, an R package that incorporates most state-of-the-art deconvolution methods, into an intuitive and extendible framework, providing a single entry point to explore, assess and disentangle gene expression data from heterogeneous samples. AVAILABILITY AND IMPLEMENTATION: The CellMix package builds on R/BioConductor and is available from http://web.cbio.uct.ac.za/∼renaud/CRAN/web/CellMix. It is currently being submitted to BioConductor. The package's vignettes notably contain additional information, examples and references. Renaud Gaujoux, Cathal Seoighe |
Bioinform. | 1 |
| 2010 | A flexible R package for nonnegative matrix factorizationabstractBACKGROUND: Nonnegative Matrix Factorization (NMF) is an unsupervised learning technique that has been applied successfully in several fields, including signal processing, face recognition and text mining. Recent applications of NMF in bioinformatics have demonstrated its ability to extract meaningful information from high-dimensional data such as gene expression microarrays. Developments in NMF theory and applications have resulted in a variety of algorithms and methods. However, most NMF implementations have been on commercial platforms, while those that are freely available typically require programming skills. This limits their use by the wider research community. RESULTS: Our objective is to provide the bioinformatics community with an open-source, easy-to-use and unified interface to standard NMF algorithms, as well as with a simple framework to help implement and test new NMF methods. For that purpose, we have developed a package for the R/BioConductor platform. The package ports public code to R, and is structured to enable users to easily modify and/or add algorithms. It includes a number of published NMF algorithms and initialization methods and facilitates the combination of these to produce new NMF strategies. Commonly used benchmark data and visualization methods are provided to help in the comparison and interpretation of the results. CONCLUSIONS: The NMF package helps realize the potential of Nonnegative Matrix Factorization, especially in bioinformatics, providing easy access to methods that have already yielded new insights in many applications. Documentation, source code and sample data are available from CRAN. Renaud Gaujoux, Cathal Seoighe |
BMC Bioinform. | 1 |