Abstract:
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Background: Mutation studies of pancreatic ductal adenocarcinoma (PDA) have cataloged a number of genes mutated at high frequencies, but also report a very large number of genes mutated in lower percentages of tumors. Result: In this project, we determined whether the genetic mutations in SB-accelerated PDA occur within a collated group of biological processes defined as gene sets. The approach considered both genes mutated in high and lower frequencies. We implemented a case-oriented, gene set enrichment analysis (CO-GSEA) on SB altered genes in PDA. Compared to traditional GSEA, CO-GSEA enables us to consider individual characteristics of mutation profiles of each PDA tumor. We identified genetic pathways with higher numbers of genetic mutations than expected by chance.
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