Elisabet Munté
5PUBLICATIONS
15CO-AUTHORS
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Publications (5)
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|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
|Dec 12, 2024
Detection of germline CNVs from gene panel data: benchmarking the state of the art.Elisabet Munté, Carla Roca, Jesús Del Valle
|Mar 14, 2023
vaRHC: an R package for semi-automation of variant classification in hereditary cancer genes according to ACMG/AMP and gene-specific ClinGen guidelines.Elisabet Munté, Lidia Feliubadaló, Marta Pineda
|Jan 27, 2021
BARD1 Pathogenic Variants are Associated with Triple-Negative Breast Cancer in a Spanish Hereditary Breast and Ovarian Cancer Cohort.Paula Rofes, Jesús Del Valle, Sara Torres-Esquius
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Frequent Collaborators
4 joint publications
Lídia Feliubadaló
3 joint publications
José Marcos Moreno-Cabrera
2 joint publications
Paula Rofes
2 joint publications
Jesús Del Valle
2 joint publications
Conxi Lázaro
1 joint publications
Gabriel Capellá
1 joint publications
Joan Brunet
1 joint publications
Jose Luis Mosquera
1 joint publications
Carla Roca
1 joint publications
Ania Alay
