Abstract
The most popular approach to explain cancer is based on the discovery of oncogenes and tumor suppressor genes as a preliminary step in estimating their impact on altered pathways. The present paper proposes a pipeline which aims at detecting “weak” or “indirect” functions impacted by Copy Number Variations (CNVs) of cancer-related genes, integrating such signals over all known oncogenes/tumor suppressor genes of a cancer type. We applied the pipeline to the task of detecting the aberrant functional effects of these alterations across ovarian cancer patients from The Cancer Genome Atlas (TCGA) data.
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Giacomini, G., Ciravegna, G., Pellegrini, M., D’Aurizio, R., Bianchini, M. (2020). A Transcriptional Study of Oncogenes and Tumor Suppressors Altered by Copy Number Variations in Ovarian Cancer. In: Chen, YW., Tanaka, S., Howlett, R., Jain, L. (eds) Innovation in Medicine and Healthcare. Smart Innovation, Systems and Technologies, vol 192. Springer, Singapore. https://doi.org/10.1007/978-981-15-5852-8_15
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DOI: https://doi.org/10.1007/978-981-15-5852-8_15
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