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Updated: Mar 19, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
Mutational patterns in oncogenes and tumour suppressors
Hanadi M Baeissa1, Graeme Benstead-Hume1, Christopher J Richardson2
1Bioinformatics Group, School of Life Sciences, University of Sussex, Falmer, Brighton, BN1 9QJ, U.K.
Cancer progression relies on gene mutations. Understanding these mutations
Area of Science:
- Oncology
- Genetics
- Bioinformatics
Background:
- Cancers arise from critical gene mutations conferring a selective advantage to tumor cells.
- Understanding these mutations is vital for cancer biology, initiation, progression, and targeted therapies.
- Assessing mutation impact on protein function and pathways is key to understanding disease contribution.
Purpose of the Study:
- To examine mutation patterns in oncogenes and tumor suppressors.
- To discuss methods for identifying cancer driver mutations.
- To introduce the MOKCa database for annotating cancer-associated protein mutations.
Main Methods:
- Analysis of mutation patterns in oncogenes and tumor suppressors.
- Review of approaches for identifying driver mutations in cancer.
- Development of an automatic pipeline for structural and functional annotation of mutated proteins.
Main Results:
- Identified mutation patterns in key cancer-related genes.
- Evaluated various strategies for pinpointing cancer-driving mutations.
- Established the MOKCa database with annotated human proteome proteins mutated in cancer.
Conclusions:
- Mutation patterns in oncogenes and tumor suppressors provide insights into cancer development.
- Identifying driver mutations is crucial for understanding cancer progression and developing therapies.
- The MOKCa database offers a valuable resource for cancer research by annotating mutated proteins.
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