Acervo - Genómica del Cáncer Comprehensive Genomic Development and validation of a clinical cancer genomic profiling test based on massively parallel DNA sequencing Validation of prostate cancer risk-related loci identified from genome-wide association studies using family -based association analysis Targeting epigenetic readers in cancer Sequence analysis of mutations and translocations across breast cancer subtypes Non-invasive genomic detection of melanoma Identification and pathway analysis of mucriRNAs with no previous involement in breast cancer Germline BRCA1 mutations increase prostate cancer risk Discovery and preclinical validation biomarkers for the non-invasive detection of breast cancer Detection of redundant fusion transcripts as biomarkers or disease-specific therapeutic targets in breast cancer A study based on whole-genome sequencing yields a rare variant at 8q24 associated with prostate cancer