Jerome Audoux
Montpellier, 34000, France
Last Updated: 09/26/2026
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Found 11 publications
Integration of Machine Learning-Based Pathogenicity Prediction and Phenotype Matching Improves Variant Prioritization in Rare Clinical Testing.
Journal: Current issues in molecular biology
Published: June 06, 2026
Clinical evaluation of a low-coverage whole-genome test for detecting homologous recombination deficiency in ovarian cancer.
Journal: European journal of cancer (Oxford, England : 1990)
Published: December 18, 2023
Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene-phenotype reassessment in clinical routine.
Journal: Genetics in medicine : official journal of the American College of Medical Genetics
Published: November 30, 2021
Kmerator Suite: design of specific k-mer signatures and automatic metadata discovery in large RNA-seq datasets.
Journal: NAR genomics and bioinformatics
Published: November 17, 2020
RNA-Seq Analysis to Detect Abnormal Fusion Transcripts Linked to Chromothripsis.
Journal: Methods in molecular biology (Clifton, N.J.)
Published: March 23, 2018
New insights into diagnosis and therapeutic options for proliferative hepatoblastoma.
Journal: Hepatology (Baltimore, Md.)
Published: July 25, 2017
DE-kupl: exhaustive capture of biological variation in RNA-seq data through k-mer decomposition.
Journal: Genome biology
Published: June 01, 2017
SimBA: A methodology and tools for evaluating the performance of RNA-Seq bioinformatic pipelines.
Journal: BMC bioinformatics
Published: January 20, 2017
On the evaluation of the fidelity of supervised classifiers in the prediction of chimeric RNAs.
Journal: BioData mining
Published: February 01, 2016
U6 snRNA Pseudogenes: Markers of Retrotransposition Dynamics in Mammals.
Journal: Molecular biology and evolution
Published: March 13, 2015
Showing 1-11 of 11
Last Updated: 09/26/2026