Lidia Feliubadaló

13PUBLICATIONS
204CO-AUTHORS
Gene expression (incl. microarray and other genome-wide approaches)Recommender systemsCancer geneticsEpigenetics (incl. genome methylation and epigenomics)Medical biotechnology not elsewhere classified
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Publications (13)

|Mar 17, 2026
Evaluation of BoostDM, a somatic variant prediction tool, for the interpretation of germline variants in hereditary cancer genes.

Elisabet Munté, Ferran Muiños, Raúl Marín

|Mar 17, 2026
Optimizing GRIDSS for clinical use: A targeted NGS filtering strategy for germline structural variant detection.

Elisabet Munté, Paula Rofes, Miriam Millán-Castillo

|Jul 05, 2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.

José M Moreno-Cabrera, Lidia Feliubadaló, Marta Pineda

|Jul 29, 2023
Choosing Variant Interpretation Tools for Clinical Applications: Context Matters.

Josu Aguirre, Natàlia Padilla, Selen Özkan

|Jul 14, 2023
ENIGMA CHEK2gether Project: A Comprehensive Study Identifies Functionally Impaired CHEK2 Germline Missense Variants Associated with Increased Breast Cancer Risk.

Lenka Stolarova, Petra Kleiblova, Petra Zemankova

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