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Pharmaceuticals (Basel, Switzerland)|July 2, 2021
cfDNA Sequencing: Technological Approaches and Bioinformatic IssuesElodie Bohers, Pierre-Julien Viailly, Fabrice Jardin
Computational and Structural Biotechnology Journal|September 21, 2020
UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Leukemia & Lymphoma|August 19, 2014
Activating somatic mutations in diffuse large B-cell lymphomas: lessons from next generation sequencing and key elements in the precision medicine eraElodie Bohers, Sylvain Mareschal, Philippe Bertrand, et al.
Bioinformatics (Oxford, England)|January 28, 2020
UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS librariesVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
BMC Cancer|August 12, 2017
A lowered 26S proteasome activity correlates with mantle lymphoma cell lines resistance to genotoxic stressKhaoula Ben Younes, Simon Body, Élodie Costé, et al.
Cancers|October 3, 2020
<i>XPO1</i><sup>E571K</sup> Mutation Modifies Exportin 1 Localisation and Interactome in B-cell LymphomaHadjer Miloudi, Élodie Bohers, François Guillonneau, et al.
Methods in Molecular Biology (Clifton, N.J.)|June 25, 2022
UMI-Varcal: A Low-Frequency Variant Caller for UMI-Tagged Paired-End Sequencing DataVincent Sater, Pierre-Julien Viailly, Thierry Lecroq, et al.
Leukemia|July 1, 2026
PD-L2 is associated with lineage-related transcriptional programs distinct from PD-L1 in primary mediastinal large B-cell lymphomaMélody Caillot, Audrey Da Rocha, Morgane Lafenêtre, et al.
Journal of Neuro-Oncology|November 16, 2024
The clinical impact of EGFR alterations in elderly glioblastoma patients: results from a real-life cohortSéréna Pulcini, Ludivine Beaussire-Trouvay, Florent Marguet, et al.
Oncotarget|July 11, 2018
New generation sequencing of targeted genes in the classical and the variant form of hairy cell leukemia highlights mutations in epigenetic regulation genesElsa Maitre, Philippe Bertrand, Catherine Maingonnat, et al.
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