2024
SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population.
Database J. Biol. Databases Curation, January, 2024

Detection of germline CNVs from gene panel data: benchmarking the state of the art.
Briefings Bioinform., 2024

2021
CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools.
Bioinform., November, 2021