Angelina Legros

Caen, 14000, France

Last Updated: 09/26/2026

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Found 14 publications

Decipher RNA isoform combinations from minigene splicing assays and massive parallel sequencing with MAGIC.

Decipher RNA isoform combinations from minigene splicing assays and massive parallel sequencing with MAGIC.

Journal: Bioinformatics (Oxford, England)

Published: June 05, 2025

Comparative Performance of a Targeted Next-Generation Sequencing Assay Against Multiplexed Digital PCR Assays in Detecting ERBB2, ESR1, and PIK3CA Mutations in Plasma Circulating Cell-Free DNA from Liquid Biopsies.

Comparative Performance of a Targeted Next-Generation Sequencing Assay Against Multiplexed Digital PCR Assays in Detecting ERBB2, ESR1, and PIK3CA Mutations in Plasma Circulating Cell-Free DNA from Liquid Biopsies.

Journal: The Journal of molecular diagnostics : JMD

Published: January 07, 2025

Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis.

Bridging the Diagnostic Gap in Hereditary Cancers with Simple, Cost-Effective, High-Throughput RNA Splicing Analysis.

Journal: The Journal of molecular diagnostics : JMD

Published: November 15, 2024

Fine mapping of RNA isoform diversity using an innovative targeted long-read RNA sequencing protocol with novel dedicated bioinformatics pipeline.

Fine mapping of RNA isoform diversity using an innovative targeted long-read RNA sequencing protocol with novel dedicated bioinformatics pipeline.

Journal: BMC genomics

Published: April 30, 2024

Validation of the Clinical Use of GIScar, an Academic-developed Genomic Instability Score Predicting Sensitivity to Maintenance Olaparib for Ovarian Cancer.

Validation of the Clinical Use of GIScar, an Academic-developed Genomic Instability Score Predicting Sensitivity to Maintenance Olaparib for Ovarian Cancer.

Journal: Clinical cancer research : an official journal of the American Association for Cancer Research

Published: March 27, 2023

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Classification of 101 BRCA1 and BRCA2 variants of uncertain significance by cosegregation study: A powerful approach.

Journal: American journal of human genetics

Published: June 15, 2021

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

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

Journal: BMC genomics

Published: July 16, 2019

Giant thermal Hall conductivity in the pseudogap phase of cuprate superconductors.

Giant thermal Hall conductivity in the pseudogap phase of cuprate superconductors.

Journal: Nature

Published: December 18, 2018

Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families.

Landscape of pathogenic variations in a panel of 34 genes and cancer risk estimation from 5131 HBOC families.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: September 06, 2017

Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.

Detecting splicing patterns in genes involved in hereditary breast and ovarian cancer.

Journal: European journal of human genetics : EJHG

Published: November 30, 2016

BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.

BRCA1 allele-specific expression in genetic predisposed breast/ovarian cancer.

Journal: Familial cancer

Published: October 27, 2016

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

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

Journal: Oncotarget

Published: May 26, 2016

Showing 1-12 of 14

Last Updated: 09/26/2026