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Céline Brochier-Armanet

dblp:96/7396 · DBLP profile ↗
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2ranked-venue papers
0as first author
1since 2021 · last 2025
0000-0003-4669-3589ORCID · reported

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
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
comparative genomics
0.412019
GeneSpy, a user-friendly and flexible genomic context visualizer · Bioinform. 2019
Bioinformatics and computational biology › genomics › genome visualization
genomic context visualization
0.412019
GeneSpy, a user-friendly and flexible genomic context visualizer · Bioinform. 2019
Bioinformatics and computational biology
genome annotation
0.112019
GeneSpy, a user-friendly and flexible genomic context visualizer · Bioinform. 2019

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

graphical user interface · 0.4
YearPublicationVenuePosition
2025 Multi-proteins similarity-based sampling to select representative genomes from large databases
abstract
BACKGROUND: Genome sequence databases are growing exponentially, but with high redundancy and uneven data quality. For these reasons, selecting representative subsets of genomes is an essential step for almost all studies. However, most current sampling approaches are biased and unable to process large datasets in a reasonable time. METHODS: Here we present MPS-Sampling (Multiple-Protein Similarity-based Sampling), a fast, scalable, and efficient method for selecting reliable and representative samples of genomes from very large datasets. Using families of homologous proteins as input, MPS-Sampling delineates homogeneous groups of genomes through two successive clustering steps. Representative genomes are then selected within these groups according to predefined or user-defined priority criteria. RESULTS: MPS-Sampling was applied to a dataset of 48 ribosomal protein families from 178,203 bacterial genomes to generate representative genome sets of various size, corresponding to a sampling of 32.17% down to 0.3% of the complete dataset. An in-depth analysis shows that the selected genomes are both taxonomically and phylogenetically representative of the complete dataset, demonstrating the relevance of the approach. CONCLUSION: MPS-Sampling provides an efficient, fast and scalable way to sample large collections of genomes in an acceptable computational time. MPS-Sampling does not rely on taxonomic information and does not require the inference of phylogenetic trees, thus avoiding the biases inherent in these approaches. As such, MPS-Sampling meets the needs of a growing number of users.
Rémi-Vinh Coudert, Jean-Philippe Charrier, Frédéric Jauffrit, Jean-Pierre Flandrois, Céline Brochier-Armanet
BMC Bioinform.5
2019 GeneSpy, a user-friendly and flexible genomic context visualizer
abstract
Summary: The exploration and comparison of genome organization is routinely used in the frame of genomic and phylogenomic analyses. As a consequence, in the past few years, various tools allowing visualizing genomic contexts have been developed. However, their use is often hampered by a lack of flexibility, particularly concerning associated databases input formats and figure customization. Here we present GeneSpy, a graphical user interface that allows the visualization and dynamic exploration of eukaryotic and prokaryotic annotated genomes. GeneSpy relies on user-friendly manageable local databases and allows the easy customization and production of figures in a multitude of formats. Availability and implementation: GeneSpy is freely available at https://lbbe.univ-lyon1.fr/GeneSpy/ for Linux, Mac OS and Windows under CeCILL license (http://www.cecill.info/licences/). It is written in Python 2.7 and depends on Matplotlib, Tkinter and Sqlite libraries. Supplementary information: Supplementary data are available at Bioinformatics online.
Pierre Simon Garcia, Frédéric Jauffrit, Christophe Grangeasse, Céline Brochier-Armanet
Bioinform.4