Somatic mutations of cell-free circulating DNA detected

Somatic mutations of cell-free circulating DNA detected by next-generation sequencing reflect the genetic changes in both germinal center B-cell-like and activated B-cell-like diffuse large B-cell lymphomas at the time of diagnosis. - Bohers E, Viailly PJ, Dubois S& al - Haematologica. 2015 Jul - PMID: 25749829

Oncogenic events rather than antigen selection pressure

Oncogenic events rather than antigen selection pressure may be the main driving forces for relapse in diffuse large B-cell lymphomas. - Rizzo D, Viailly PJ, Mareschal S & al - Am J Hematol. 2017 Jan - PMID: 27737507

A recurrent clonally distinct Burkitt lymphoma case

A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis. - Penther D, Viailly PJ, Latour S & al - Genes Chromosomes Cancer. 2019 Aug - PMID: 30779244

Non-invasive monitoring of diffuse large B-cell lymphoma

Non-invasive monitoring of diffuse large B-cell lymphoma by cell-free DNA high-throughput targeted sequencing: analysis of a prospective cohort. - Bohers E, Viailly PJ, Becker S & al - Blood Cancer J. 2018 Aug 1 - PMID: 30069017

Somatic mutations of cell-free circulating DNA

Somatic mutations of cell-free circulating DNA detected by targeted next-generation sequencing and digital droplet PCR in classical Hodgkin lymphoma. Bessi L, Viailly PJ, Bohers E & al - Leuk Lymphoma. 2019 Feb - PMID: 30068243

Biological and Clinical Relevance of Associated Genomic Alterations

Biological and Clinical Relevance of Associated Genomic Alterations in MYD88 L265P and non-L265P-Mutated Diffuse Large B-Cell Lymphoma: Analysis of 361 Cases. Dubois S, Viailly PJ, Bohers E & al - Clin Cancer Res. 2017 May 1 - PMID: 27923841

Next-Generation Sequencing

Next-Generation Sequencing in Diffuse Large B-Cell Lymphoma Highlights Molecular Divergence and Therapeutic Opportunities: a LYSA Study. / Dubois S, Viailly PJ, Mareschal S & al - Clin Cancer Res. 2016 Jun 15 - PMID: 26819451

UMI-Gen

UMI-Gen: A UMI-based read simulator for variant calling evaluation in paired-end sequencing NGS libraries. - Sater V, Viailly PJ, Lecroq T & al - Comput Struct Biotechnol J. 2020 Aug 27 - PMID: 32952940

UMI-VarCal

UMI-VarCal: a new UMI-based variant caller that efficiently improves low-frequency variant detection in paired-end sequencing NGS libraries. - Sater V, Viailly PJ, Lecroq T & al - Bioinformatics. 2020 May 1 - PMID: 31985795

Combining gene expression profiling and machine learning

Combining gene expression profiling and machine learning to diagnose B-cell non-Hodgkin lymphoma. Bobée V, Drieux F, Marchand V, Sater V, Veresezan L, Picquenot JM, Viailly PJ, Lanic MD, Viennot M, Bohers E, Oberic L, Copie-Bergman C, Molina TJ, Gaulard P, Haioun C, Salles G, Tilly H, Jardin F, Ruminy P. Blood Cancer J. 2020 May 22;10(5):59. doi: 10.1038/s41408-020-0322-5. PMID: 32444689