CLEAR-test: Combining inference for differential expression and variability in microarray data analysis. - Joan Valls; Mònica Grau; Xavier Solé; Pilar Hernández; David Montaner; Joaquín Dopazo; Miguel A. Peinado; Gabriel Capellá; Víctor Moreno; Miguel Angel Pujana (J. Biomed. Informatics, 2008)

CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools. - José Marcos Moreno-Cabrera; Jesús del Valle; Elisabeth Castellanos; Lidia Feliubadaló; Marta Pineda; Eduard Serra; Gabriel Capellá; Conxi Lázaro; Bernat Gel (Bioinform., 2021)

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; Eva Tornero; Maribel González; José Marcos Moreno-Cabrera; Carla Roca; Joan Bales Rubio; Laura Arnaldo; Gabriel Capellá; Jose Luis Mosquera; Conxi Lázaro (Bioinform., 2023)

SpadaHC: a database to improve the classification of variants in hereditary cancer genes in the Spanish population. - José Marcos Moreno-Cabrera; Lidia Feliubadaló; Marta Pineda; Patricia Prada-Dacasa; Mireia Ramos-Muntada; Jesús del Valle; Joan Brunet; Bernat Gel; María Currás-Freixes; Bruna Calsina; Milton E. Salazar-Hidalgo; Marta Rodríguez-Balada; et al. (Database J. Biol. Databases Curation, 2024)