Frédéric Chalmel

dblp:82/2257 · DBLP profile ↗
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5ranked-venue papers
2as first author
0since 2021 · last 2019
0000-0002-0535-3628ORCID · verified

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

Applied, interdisciplinary, general and emerging computing · 5 · 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
4 papers
Bioinformatics and computational biology · 100%

Topics — the 13 heaviest of 13, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology
biological database
0.722019
The ReproGenomics Viewer: a multi-omics and cross-species resource compatible with single-cell studies for the reproductive science community · Bioinform. 2019
TOXsIgN: a cross-species repository for toxicogenomic signatures · Bioinform. 2018
Bioinformatics and computational biology
multi-omics data integration
0.412019
The ReproGenomics Viewer: a multi-omics and cross-species resource compatible with single-cell studies for the reproductive science community · Bioinform. 2019
Bioinformatics and computational biology
transcriptomics
0.412019
The ReproGenomics Viewer: a multi-omics and cross-species resource compatible with single-cell studies for the reproductive science community · Bioinform. 2019
Bioinformatics and computational biology › genomics
toxicogenomics
0.312018
TOXsIgN: a cross-species repository for toxicogenomic signatures · Bioinform. 2018
Bioinformatics and computational biology
clustering and visualization
0.112005
goCluster integrates statistical analysis and functional interpretation of microarray expression data · Bioinform. 2005
Bioinformatics and computational biology › functional genomics
functional enrichment analysis
0.112005
goCluster integrates statistical analysis and functional interpretation of microarray expression data · Bioinform. 2005
Bioinformatics and computational biology
gene expression analysis
0.112005
goCluster integrates statistical analysis and functional interpretation of microarray expression data · Bioinform. 2005
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
gene ontology analysis
0.112005
goCluster integrates statistical analysis and functional interpretation of microarray expression data · Bioinform. 2005
Bioinformatics and computational biology › protein function prediction
gene ontology annotation
0.112005
GOAnno: GO annotation based on multiple alignment · Bioinform. 2005
Bioinformatics and computational biology › gene expression analysis
microarray data analysis
0.112005
goCluster integrates statistical analysis and functional interpretation of microarray expression data · Bioinform. 2005
Bioinformatics and computational biology
protein function prediction
0.112005
GOAnno: GO annotation based on multiple alignment · Bioinform. 2005
Bioinformatics and computational biology
multiple sequence alignment
0.012005
GOAnno: GO annotation based on multiple alignment · Bioinform. 2005
Bioinformatics and computational biology
sequence analysis
0.012005
GOAnno: GO annotation based on multiple alignment · Bioinform. 2005

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

manual curation · 0.4enrichment analysis · 0.3multiple testing correction · 0.1hypergeometric test · 0.1cross-validation · 0.1clustering · 0.1annotation propagation · 0.1
YearPublicationVenuePosition
2019 The ReproGenomics Viewer: a multi-omics and cross-species resource compatible with single-cell studies for the reproductive science community
abstract
MOTIVATION: Recent advances in transcriptomics have enabled unprecedented insight into gene expression analysis at a single-cell resolution. While it is anticipated that the number of publications based on such technologies will increase in the next decade, there is currently no public resource to centralize and enable scientists to explore single-cell datasets published in the field of reproductive biology. RESULTS: Here, we present a major update of the ReproGenomics Viewer, a cross-species and cross-technology web-based resource of manually-curated sequencing datasets related to reproduction. The redesign of the ReproGenomics Viewer's architecture is accompanied by significant growth of the database content including several landmark single-cell RNA-sequencing datasets. The implementation of additional tools enables users to visualize and browse the complex, high-dimensional data now being generated in the reproductive field. AVAILABILITY AND IMPLEMENTATION: The ReproGenomics Viewer resource is freely accessible at http://rgv.genouest.org. The website is implemented in Python, JavaScript and MongoDB, and is compatible with all major browsers. Source codes can be downloaded from https://github.com/fchalmel/RGV. SUPPLEMENTARY INFORMATION: Supplementary data are available at Bioinformatics online.
Thomas A. Darde, Estelle Lecluze, Aurélie Lardenois, Isabelle Stévant, Nathan Alary, Frank Tüttelmann, Olivier Collin, Serge Nef, Bernard Jégou, Antoine D. Rolland, Frédéric Chalmel
Bioinform.11
2018 TOXsIgN: a cross-species repository for toxicogenomic signatures
abstract
Motivation: At the same time that toxicologists express increasing concern about reproducibility in this field, the development of dedicated databases has already smoothed the path toward improving the storage and exchange of raw toxicogenomic data. Nevertheless, none provides access to analyzed and interpreted data as originally reported in scientific publications. Given the increasing demand for access to this information, we developed TOXsIgN, a repository for TOXicogenomic sIgNatures. Results: The TOXsIgN repository provides a flexible environment that facilitates online submission, storage and retrieval of toxicogenomic signatures by the scientific community. It currently hosts 754 projects that describe more than 450 distinct chemicals and their 8491 associated signatures. It also provides users with a working environment containing a powerful search engine as well as bioinformatics/biostatistics modules that enable signature comparisons or enrichment analyses. Availability and implementation: The TOXsIgN repository is freely accessible at http://toxsign.genouest.org. Website implemented in Python, JavaScript and MongoDB, with all major browsers supported. Supplementary information: Supplementary data are available at Bioinformatics online.
Thomas A. Darde, Pierre Gaudriault, Rémi Beranger, Clément Lancien, Annaëlle Caillarec-Joly, Olivier Sallou, Nathalie Bonvallot, Cécile Chevrier, Séverine Mazaud-Guittot, Bernard Jégou, Olivier Collin, Emmanuelle Becker, Antoine D. Rolland, Frédéric Chalmel
Bioinform.14
2008 The Annotation, Mapping, Expression and Network (AMEN) suite of tools for molecular systems biology
abstract
BACKGROUND: High-throughput genome biological experiments yield large and multifaceted datasets that require flexible and user-friendly analysis tools to facilitate their interpretation by life scientists. Many solutions currently exist, but they are often limited to specific steps in the complex process of data management and analysis and some require extensive informatics skills to be installed and run efficiently. RESULTS: We developed the Annotation, Mapping, Expression and Network (AMEN) software as a stand-alone, unified suite of tools that enables biological and medical researchers with basic bioinformatics training to manage and explore genome annotation, chromosomal mapping, protein-protein interaction, expression profiling and proteomics data. The current version provides modules for (i) uploading and pre-processing data from microarray expression profiling experiments, (ii) detecting groups of significantly co-expressed genes, and (iii) searching for enrichment of functional annotations within those groups. Moreover, the user interface is designed to simultaneously visualize several types of data such as protein-protein interaction networks in conjunction with expression profiles and cellular co-localization patterns. We have successfully applied the program to interpret expression profiling data from budding yeast, rodents and human. CONCLUSION: AMEN is an innovative solution for molecular systems biological data analysis freely available under the GNU license. The program is available via a website at the Sourceforge portal which includes a user guide with concrete examples, links to external databases and helpful comments to implement additional functionalities. We emphasize that AMEN will continue to be developed and maintained by our laboratory because it has proven to be extremely useful for our genome biological research program.
Frédéric Chalmel, Michael Primig
BMC Bioinform.1
2005 GOAnno: GO annotation based on multiple alignment
abstract
UNLABELLED: GOAnno is a web tool that automatically annotates proteins according to the Gene Ontology (GO) using evolutionary information available in hierarchized multiple alignments. GO terms present in the aligned functional subfamily can be cross-validated and propagated to obtain highly reliable predicted GO annotation based on the GOAnno algorithm. AVAILABILITY: The web tool and a reduced version for local installation are freely available at http://igbmc.u-strasbg.fr/GOAnno/GOAnno.html SUPPLEMENTARY INFORMATION: The website supplies a detailed explanation and illustration of the algorithm at http://igbmc.u-strasbg.fr/GOAnno/GOAnnoHelp.html.
Frédéric Chalmel, Aurélie Lardenois, Julie Dawn Thompson, Jean Muller, José-Alain Sahel, Thierry Léveillard, Olivier Poch
Bioinform.1
2005 goCluster integrates statistical analysis and functional interpretation of microarray expression data
abstract
MOTIVATION: Several tools that facilitate the interpretation of transcriptional profiles using gene annotation data are available but most of them combine a particular statistical analysis strategy with functional information. goCluster extends this concept by providing a modular framework that facilitates integration of statistical and functional microarray data analysis with data interpretation. RESULTS: goCluster enables scientists to employ annotation information, clustering algorithms and visualization tools in their array data analysis and interpretation strategy. The package provides four clustering algorithms and GeneOntology terms as prototype annotation data. The functional analysis is based on the hypergeometric distribution whereby the Bonferroni correction or the false discovery rate can be used to correct for multiple testing. The approach implemented in goCluster was successfully applied to interpret the results of complex mammalian and yeast expression data obtained with high density oligonucleotide microarrays (GeneChips). AVAILABILITY: goCluster is available via the BioConductor portal at www.bioconductor.org. The software package, detailed documentation, user- and developer guides as well as other background information are also accessible via a web portal at http://www.bioz.unibas.ch/gocluster CONTACT: [email protected]
Gunnar Wrobel, Frédéric Chalmel, Michael Primig
Bioinform.2