Gabriel Capellá
Orcid: 0000-0002-4669-7320
According to our database1,
Gabriel Capellá
authored at least 4 papers
between 2008 and 2024.
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Bibliography
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
2023
vaRHC: an R package for semi-automation of variant classification in hereditary cancer genes according to ACMG/AMP and gene-specific ClinGen guidelines.
Bioinform., 2023
2021
CNVfilteR: an R/Bioconductor package to identify false positives produced by germline NGS CNV detection tools.
Bioinform., November, 2021
2008
CLEAR-test: Combining inference for differential expression and variability in microarray data analysis.
J. Biomed. Informatics, 2008