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Stéphane Le Crom

dblp:33/6934 · DBLP profile ↗
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7ranked-venue papers
0as first author
0since 2021 · last 2018
0000-0002-0534-7797ORCID · verified

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

Applied, interdisciplinary, general and emerging computing · 7

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%
Computer architecture, parallel and distributed computing, and storage systems
1 paper
Parallel and multicore computing · 100%

Topics — the 8 heaviest of 9, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › sequence analysis
sequencing data processing
0.312017
Aozan: an automated post-sequencing data-processing pipeline · Bioinform. 2017
Bioinformatics and computational biology › sequence analysis
high-throughput sequencing data analysis
0.112012
Eoulsan: a cloud computing-based framework facilitating high throughput sequencing analyses · Bioinform. 2012
Bioinformatics and computational biology
genomics
0.112009
Selection of oligonucleotides for whole-genome microarrays with semi-automatic update · Bioinform. 2009
Bioinformatics and computational biology
microarray probe design
0.112009
Selection of oligonucleotides for whole-genome microarrays with semi-automatic update · Bioinform. 2009
Bioinformatics and computational biology › sequence analysis › primer and probe design
oligonucleotide probe selection
0.112009
Selection of oligonucleotides for whole-genome microarrays with semi-automatic update · Bioinform. 2009
Bioinformatics and computational biology › sequence analysis › sequencing data processing
sequencing quality control
0.112017
Aozan: an automated post-sequencing data-processing pipeline · Bioinform. 2017
Parallel and multicore computing › data-parallel programming
mapreduce
0.012012
Eoulsan: a cloud computing-based framework facilitating high throughput sequencing analyses · Bioinform. 2012
Bioinformatics and computational biology
genome annotation
0.012009
Selection of oligonucleotides for whole-genome microarrays with semi-automatic update · Bioinform. 2009

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

mapreduce · 0.3hadoop · 0.3semi-automatic update · 0.1automated validation testing · 0.1
YearPublicationVenuePosition
2018 Meet-U: Educating through research immersion
abstract
We present a new educational initiative called Meet-U that aims to train students for collaborative work in computational biology and to bridge the gap between education and research. Meet-U mimics the setup of collaborative research projects and takes advantage of the most popular tools for collaborative work and of cloud computing. Students are grouped in teams of 4-5 people and have to realize a project from A to Z that answers a challenging question in biology. Meet-U promotes "coopetition," as the students collaborate within and across the teams and are also in competition with each other to develop the best final product. Meet-U fosters interactions between different actors of education and research through the organization of a meeting day, open to everyone, where the students present their work to a jury of researchers and jury members give research seminars. This very unique combination of education and research is strongly motivating for the students and provides a formidable opportunity for a scientific community to unite and increase its visibility. We report on our experience with Meet-U in two French universities with master's students in bioinformatics and modeling, with protein-protein docking as the subject of the course. Meet-U is easy to implement and can be straightforwardly transferred to other fields and/or universities. All the information and data are available at www.meet-u.org.
Nika Abdollahi, Alexandre Albani, Éric Anthony, Agnes Baud, Mélissa Cardon, Robert Clerc, Dariusz Czernecki, Romain Conte, Laurent David, Agathe Delaune, Samia Djerroud, Pauline Fourgoux, Nadège Guiglielmoni, Jeanne Laurentie, Nathalie Lehmann, Camille Lochard, Rémi Montagne, Vasiliki Myrodia, Vaitea Opuu, Elise Parey, Lélia Polit, Sylvain Privé, Chloé Quignot, Maria Ruiz-Cuevas, Mariam Sissoko, Nicolas Sompairac, Audrey Vallerix, Violaine Verrecchia, Marc Delarue, Raphaël Guérois, Yann Ponty, Sophie Sacquin-Mora, Alessandra Carbone, Christine Froidevaux, Stéphane Le Crom, Olivier Lespinet, Martin Weigt, Samer Abboud, Juliana S. Bernardes, Guillaume Bouvier, Chloé Dequeker, Arnaud Ferré, Patrick Fuchs, Gaëlle Lelandais, Pierre Poulain, Hugues Richard, Hugo Schweke, Elodie Laine, Anne Lopes
PLoS Comput. Biol.35
2017 Aozan: an automated post-sequencing data-processing pipeline
abstract
MOTIVATION: Data management and quality control of output from Illumina sequencers is a disk space- and time-consuming task. Thus, we developed Aozan to automatically handle data transfer, demultiplexing, conversion and quality control once a run has finished. This software greatly improves run data management and the monitoring of run statistics via automatic emails and HTML web reports. AVAILABILITY AND IMPLEMENTATION: Aozan is implemented in Java and Python, supported on Linux systems, and distributed under the GPLv3 License at: http://www.outils.genomique.biologie.ens.fr/aozan/ . Aozan source code is available on GitHub: https://github.com/GenomicParisCentre/aozan . CONTACT: [email protected].
Sandrine Perrin, Cyril Firmo, Sophie Lemoine, Stéphane Le Crom, Laurent Jourdren
Bioinform.4
2013 A comprehensive evaluation of normalization methods for Illumina high-throughput RNA sequencing data analysis
abstract
During the last 3 years, a number of approaches for the normalization of RNA sequencing data have emerged in the literature, differing both in the type of bias adjustment and in the statistical strategy adopted. However, as data continue to accumulate, there has been no clear consensus on the appropriate normalization method to be used or the impact of a chosen method on the downstream analysis. In this work, we focus on a comprehensive comparison of seven recently proposed normalization methods for the differential analysis of RNA-seq data, with an emphasis on the use of varied real and simulated datasets involving different species and experimental designs to represent data characteristics commonly observed in practice. Based on this comparison study, we propose practical recommendations on the appropriate normalization method to be used and its impact on the differential analysis of RNA-seq data.
Marie-Agnès Dillies, Andrea Rau, Julie Aubert, Christelle Hennequet-Antier, Marine Jeanmougin, Nicolas Servant, Céline Keime, Guillemette Marot, David Castel, Jordi Estelle, Gregory Guernec, Bernd Jagla, Luc Jouneau, Denis Laloë, Caroline Le Gall, Brigitte Schaeffer, Stéphane Le Crom, Mickaël Guedj, Florence Jaffrézic
Briefings Bioinform.17
2012 Eoulsan: a cloud computing-based framework facilitating high throughput sequencing analyses
abstract
UNLABELLED: We developed a modular and scalable framework called Eoulsan, based on the Hadoop implementation of the MapReduce algorithm dedicated to high-throughput sequencing data analysis. Eoulsan allows users to easily set up a cloud computing cluster and automate the analysis of several samples at once using various software solutions available. Our tests with Amazon Web Services demonstrated that the computation cost is linear with the number of instances booked as is the running time with the increasing amounts of data. AVAILABILITY AND IMPLEMENTATION: Eoulsan is implemented in Java, supported on Linux systems and distributed under the LGPL License at: http://transcriptome.ens.fr/eoulsan/
Laurent Jourdren, Maria Bernard, Marie-Agnès Dillies, Stéphane Le Crom
Bioinform.4
2009 Selection of oligonucleotides for whole-genome microarrays with semi-automatic update
abstract
Abstract Summary: Oligonucleotide microarray probes are designed to match specific transcripts present in databases that are regularly updated. As a consequence probes should be checked every new database release. We thus developed an informatics tool allowing the semi-automatic update of probe collections of long oligonucleotides and applied it to the mouse RefSeq database. Availability: http://www.bio.espci.fr/sol/ Contact: [email protected] Supplementary information: Supplementary data are available at http://www.bio.espci.fr/sol/
G. Golfier, Sophie Lemoine, A. van Miltenberg, A. Bendjoudi, J. Rossier, Stéphane Le Crom, Marie-Claude Potier
Bioinform.6
2006 Goulphar: rapid access and expertise for standard two-color microarray normalization methods
abstract
BACKGROUND: Raw data normalization is a critical step in microarray data analysis because it directly affects data interpretation. Most of the normalization methods currently used are included in the R/BioConductor packages but it is often difficult to identify the most appropriate method. Furthermore, the use of R commands for functions and graphics can introduce mistakes that are difficult to trace. We present here a script written in R that provides a flexible means of access to and monitoring of data normalization for two-color microarrays. This script combines the power of BioConductor and R analysis functions and reduces the amount of R programming required. RESULTS: Goulphar was developed in and runs using the R language and environment. It combines and extends functions found in BioConductor packages (limma and marray) to correct for dye biases and spatial artifacts. Goulphar provides a wide range of optional and customizable filters for excluding incorrect signals during the pre-processing step. It displays informative output plots, enabling the user to monitor the normalization process, and helps adapt the normalization method appropriately to the data. All these analyses and graphical outputs are presented in a single PDF report. CONCLUSION: Goulphar provides simple, rapid access to the power of the R/BioConductor statistical analysis packages, with precise control and visualization of the results obtained. Complete documentation, examples and online forms for setting script parameters are available from http://transcriptome.ens.fr/goulphar/.
Sophie Lemoine, Florence Combes, Nicolas Servant, Stéphane Le Crom
BMC Bioinform.4
2005 Doelan: a solution for quality control monitoring of microarray production
abstract
SUMMARY: Doelan is an automated tool designed to monitor the quality of DNA microarray production. The software executes a series of quality control tests on hybridizations to validate batches of chips. The reports generated by Doelan should help microarray platforms aiming at quality labels, such as ISO 9001 certification. The Doelan application is written in Java and works with a plug-in system that allows everyone to add custom validation tests. AVAILABILITY: The Doelan application is distributed under the GNU General Public License at http://transcriptome.ens.fr/doelan/
Laurent Jourdren, Stéphane Le Crom
Bioinform.2