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Audrey Bihouée

dblp:96/9181 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2025
0000-0002-8689-2083ORCID · corroborated

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

Applied, interdisciplinary, general and emerging computing · 2 · 1 since 2021

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
2 papers
Bioinformatics and computational biology · 100%

Topics — the 5 heaviest of 5, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › systems biology › metabolic network analysis
flux analysis
0.912025
HUMESS: integrating quantitative transcriptomic analysis and metabolic modeling to unveil condition-specific gene signatures · Bioinform. 2025
Bioinformatics and computational biology › systems biology
metabolic network modeling
0.912025
HUMESS: integrating quantitative transcriptomic analysis and metabolic modeling to unveil condition-specific gene signatures · Bioinform. 2025
Bioinformatics and computational biology
transcriptomics
0.912025
HUMESS: integrating quantitative transcriptomic analysis and metabolic modeling to unveil condition-specific gene signatures · Bioinform. 2025
Bioinformatics and computational biology
gene expression analysis
0.112011
MADGene: retrieval and processing of gene identifier lists for the analysis of heterogeneous microarray datasets · Bioinform. 2011
Bioinformatics and computational biology › functional genomics › functional enrichment analysis
gene set enrichment analysis
0.112011
MADGene: retrieval and processing of gene identifier lists for the analysis of heterogeneous microarray datasets · Bioinform. 2011

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

genome-scale metabolic modeling · 0.9flux analysis · 0.9meta-analysis · 0.1
YearPublicationVenuePosition
2025 HUMESS: integrating quantitative transcriptomic analysis and metabolic modeling to unveil condition-specific gene signatures
abstract
SUMMARY: Transcriptomic analysis is a key tool for exploring gene expression, but the complexity of biological systems often limits its insights. In particular, the lack of intermodal or multi-layered analysis hinders the ability to fully capture key cellular functions such as metabolism from transcriptomic data alone. Here, we introduce a novel approach that informs transcriptomic data analysis with metabolic network modeling to address this. Unlike traditional methods, HUman MEtabolism Specific Signature (HUMESS) uses genome-scale metabolic modeling and flux analysis to highlight reactions and involved genes based on their metabolic significance, offering a deeper understanding of transcriptomic data. Our computational pipeline, supported by a user-friendly Rshiny application, enhances gene expression analysis by uncovering metabolic phenotypic signatures. AVAILABILITY AND IMPLEMENTATION: HUMESS is open source and available under GitLab https://gitlab.univ-nantes.fr/bird_pipeline_registry/humess with the complete documentation available at https://gitlab.univ-nantes.fr/bird_pipeline_registry/humess/-/wikis/Home. A zenodo archive is also available at the following DOI: https://doi.org/10.5281/zenodo.15487717. An RShiny application has been developed to facilitate the exploration and analysis of HUMESS's results. The app is available online at the following address: https://shiny-bird.univ-nantes.fr/app/shinymess but can also be installed locally, available under GitLab https://gitlab.univ-nantes.fr/pare-l/shinymess.
Louis Paré, Philippe Bordron, Laurent David, Maxime Mahé, Audrey Bihouée, Damien Eveillard
Bioinform.5
2011 MADGene: retrieval and processing of gene identifier lists for the analysis of heterogeneous microarray datasets
abstract
UNLABELLED: MADGene is a software environment comprising a web-based database and a java application. This platform aims at unifying gene identifiers (ids) and performing gene set analysis. MADGene allows the user to perform inter-conversion of clone and gene ids over a large range of nomenclatures relative to 17 species. We propose a set of 23 functions to facilitate the analysis of gene sets and we give two microarray applications to show how MADGene can be used to conduct meta-analyses. AVAILABILITY: The MADGene resources are freely available online from http://www.madtools.org, a website dedicated to the analysis and annotation of DNA microarray data.
Daniel Baron, Audrey Bihouée, Raluca Teusan, Emeric Dubois, Frédérique Savagner, Marja Steenman, Rémi Houlgatte, Gérard Ramstein
Bioinform.2