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How to explore cancer-related mutations using NGS
EP37209
Poster Title: How to explore cancer-related mutations using NGS
Submitted on 05 May 2021
Author(s): CD Genomics
Affiliations: CD Genomics
Poster Views: 79
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Poster Information
Abstract: Cancer is primarily caused by genetic alterations, which may be inherited or acquired in somatic cells. These alterations in oncogenes, tumor suppressor genes, or DNA repair genes may enable cells to evade growth inhibition in response to growth-inhibitory signals, leading to the development of a tumor. Further mutations may occur in the progeny of the cancer cell, leading to the development of tumor cell invasion and metastasis. The application of NGS provides a high-resolution and global view of the cancer genome in a high-throughput manner, which has revealed a number of novel cancer-related genes and pathways. https://www.cd-genomics.com/Summary: Cancer is primarily caused by genetic alterations, which may be inherited or acquired in somatic cells. These alterations in oncogenes, tumor suppressor genes, or DNA repair genes may enable cells to evade growth inhibition in response to growth-inhibitory signals, leading to the development of a tumor. References: https://www.cd-genomics.com/Report abuse »
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