Novel approach to functional SNPs discovery from genome-wide data reveals promising variants for colon cancer risk

Research output: Contribution to journal › Article › peer-review

Allele-specific events, Colorectal cancer, Functional variants, Gene regulation, SNPs, colorectal cancer, gene regulation, allele-specific events, functional variants, SUPPRESSOR, MICRORNAS, IDENTIFICATION, EPIGENETICS, SART3, TUMOR-REJECTION ANTIGEN, GENES, ASSOCIATION, EXPRESSION, RNA-SEQ DATA, Humans, Male, Polymorphism, Single Nucleotide/genetics, Genome, Human/genetics, Female, Genetic Predisposition to Disease, Genome-Wide Association Study, Colonic Neoplasms/genetics, Gene Frequency, HCT116 Cells, Risk Factors, Genotype, Alleles

ID: 12417563