Comparing algorithms that search for cancer mutations

IMAGE: Adam Godzik, Ph.D., is director of the Bioinformatics and Structural Biology Program at Sanford Burnham Prebys Medical Discovery Institute.
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Credit: Bil Zelman

Sanford Burnham Prebys Medical Discovery Institute (SBP) has undertaken the first-ever comparative analysis of a newly emerging category of algorithms that mine genetic information in cancer databases by focusing on internal gene structure (subgene resolution algorithms), in contrast to classical approaches that focus on genes treated as single units. These powerful data-sifting tools are helping untangle the complexity of cancer, and find previously unidentified mutations that are important in creating cancer cells.

The study, published today in Nature Methods, reviews, classifies and describes the strengths and weaknesses of more than 20 algorithms developed by independent research groups.

“Despite the increasing availability of high-resolution genome sequences, a common assumption is to consider a gene as a single unit,” explains Adam Godzik, Ph.D., director of the Bioinformatics and Structural Biology Program at SBP, and senior author of the study. “However, there are a number of events, such as single site DNA substitutions and splicing variants that can occur within a gene–at the subgene level. Subgene algorithms provide a high-resolution view that can explain why different mutations in the same gene can lead to distinct phenotypes, depending on how they impact specific protein regions.

“A good example of how different subgene mutations influence cancer is the NOTCH1 gene,” says Godzik. “Mutations in certain regions of NOTCH1 cause it to act as a tumor suppressor in lung, skin and head and neck cancers. But mutations in a different region can promote chronic lymphocytic leukemia and T cell acute lymphoblastic leukemia. So it’s incorrect to assume that mutations in a gene will have the same consequences regardless of their location.”

The study…

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