Dominique Vaur

SpliceLauncher: a tool for detection, annotation and relative quantification of alternative junctions from RNAseq data

Raphaël Leman, Valentin Harter, Alexandre Atkinson, 2019, Bioinform..

Multiple sequence variants of BRCA2 exon 7 alter splicing regulation

Etienne Rouleau, Dominique Vaur, Sophie Krieger, 2012, Journal of Medical Genetics.

OutLyzer: software for extracting low-allele-frequency tumor mutations from sequencing background noise in clinical practice

Dominique Vaur, Sophie Krieger, Baptiste Brault, 2016, Oncotarget.

BRCA Share: A Collection of Clinical BRCA Gene Variants

Christophe Béroud, Dominique Vaur, Izabela Karbassi, 2016, Human mutation.

Contribution of bioinformatics predictions and functional splicing assays to the interpretation of unclassified variants of the BRCA genes

Dominique Vaur, Sophie Krieger, Marie-Pierre Buisine, 2011, European Journal of Human Genetics.

Stereotyped patterns of somatic hypermutation in subsets of patients with chronic lymphocytic leukemia: implications for the role of antigen selection in leukemogenesis.

Nikolaos Laoutaris, Kostas Stamatopoulos, Dominique Vaur, 2007, Blood.

Assessment of branch point prediction tools to predict physiological branch points and their alteration by variants

Amanda B. Spurdle, Raphaël Leman, Marine Guillaud-Bataille, 2020, BMC Genomics.