Methods, tools, and computational environment for network-based analysis of biological data
Author: Petrov, Iurii
Date: 2023-03-22
Location: Ragnar Granit, Biomedicum, Solnavägen 9, Karolinska Institutet, Solna
Time: 09.00
Department: Inst för mikrobiologi, tumör- och cellbiologi / Dept of Microbiology, Tumor and Cell Biology
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Thesis (703.8Kb)
Abstract
Cancer currently affects more than 18 million persons world-wide annually. It is a leading cause of death and so far, only 60% cure rate can be reached within the most developed health care systems. The nature of cancer has been a mystery for centuries, until discoveries during recent decades shed light on the underlying molecular events. This depended on the progress in understanding cell and tissue biology, developments of molecular technologies and of -omics technologies. Cancer has then emerged as a highly heterogeneous disease, however with some very basic mechanistic features common to all cancers. To deal with the complexity of causes and consequences of pathological changes in the molecular machinery, methods and tools of network analysis can be helpful. Complexity of this task requires easy-to-use tools, which allow researchers and clinicians with no background in computer science to perform network analysis.
Paper I describes a web-based framework for network enrichment analysis (NEA), using previously developed algorithm and code. The developed platform introduces functionality for a researcher to use data pre-downloaded from various popular databases as well as own data, perform NEA and obtain statistical estimations, export results in different formats for publications or further use in research pipeline.
Paper II presents development of another web server, which provided vast opportunities for exploration and integrated analysis of multiple public cancer datasets that describe in vitro and in vivo sample collections. The web server linked molecular data at the single gene level, phenotype and pharmacological response variables, as well as pathway level variables calculated with NEA and connected to the framework presented in Paper I. Researchers can use the platform for creating multivariate models based on raw or pre-processed data from various sources, visualize created models, estimate their performance and compare them, export models for further usage in own research environments.
Paper III demonstrates NEAdriver, a practical application of NEA to probabilistic evaluation of driver roles of mutations reported in ten cancer cohorts. NEAdriver results are compared with cancer gene sets produced by other, both network analysis and network-free methods. The paper demonstrated ability of NEA to be used directly for discovering novel driver genes as well as being used in combination with other methods. In order to demonstrate benefits of using NEA, some rare cancer types and types with low mutation burden were used.
Paper IV is a manuscript evaluating performance of most representative methods of network analysis across methods’ parameters, functional ontologies and network versions. This study emphasizes discovery of novel functional associations for known genes, as opposed to previous tests dominated by a few “gold standard” genes which were well characterized previously. We performed the analysis in the context of various topological properties of networks, pathways of interest, and genes. It employed both existing, widely used topological metrics and a number of novel ones developed for this analysis.
Paper I describes a web-based framework for network enrichment analysis (NEA), using previously developed algorithm and code. The developed platform introduces functionality for a researcher to use data pre-downloaded from various popular databases as well as own data, perform NEA and obtain statistical estimations, export results in different formats for publications or further use in research pipeline.
Paper II presents development of another web server, which provided vast opportunities for exploration and integrated analysis of multiple public cancer datasets that describe in vitro and in vivo sample collections. The web server linked molecular data at the single gene level, phenotype and pharmacological response variables, as well as pathway level variables calculated with NEA and connected to the framework presented in Paper I. Researchers can use the platform for creating multivariate models based on raw or pre-processed data from various sources, visualize created models, estimate their performance and compare them, export models for further usage in own research environments.
Paper III demonstrates NEAdriver, a practical application of NEA to probabilistic evaluation of driver roles of mutations reported in ten cancer cohorts. NEAdriver results are compared with cancer gene sets produced by other, both network analysis and network-free methods. The paper demonstrated ability of NEA to be used directly for discovering novel driver genes as well as being used in combination with other methods. In order to demonstrate benefits of using NEA, some rare cancer types and types with low mutation burden were used.
Paper IV is a manuscript evaluating performance of most representative methods of network analysis across methods’ parameters, functional ontologies and network versions. This study emphasizes discovery of novel functional associations for known genes, as opposed to previous tests dominated by a few “gold standard” genes which were well characterized previously. We performed the analysis in the context of various topological properties of networks, pathways of interest, and genes. It employed both existing, widely used topological metrics and a number of novel ones developed for this analysis.
List of papers:
I. Jeggari A, Alekseenko Z, Petrov I, Dias JM, Ericson J, Alexeyenko A. EviNet: a web platform for network enrichment analysis with flexible definition of gene sets. Nucleic Acids Res. 2018 Jul 2;46(W1):W163-W170.
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II. Petrov I, Alexeyenko A. EviCor: Interactive Web Platform for Exploration of Molecular Features and Response to Anti-cancer Drugs. J Mol Biol. 2022 Jun 15;434(11):167528.
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III. Petrov I., Alexeyenko A. Individualized discovery of rare cancer drivers in global network context. eLife. 2022;11:e74010.
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IV. Petrov I., Alexeyenko A. Comparative performance of network versions, algorithms, and topological properties while discovering novel disease genes. [Manuscript]
I. Jeggari A, Alekseenko Z, Petrov I, Dias JM, Ericson J, Alexeyenko A. EviNet: a web platform for network enrichment analysis with flexible definition of gene sets. Nucleic Acids Res. 2018 Jul 2;46(W1):W163-W170.
Fulltext (DOI)
Pubmed
View record in Web of Science®
II. Petrov I, Alexeyenko A. EviCor: Interactive Web Platform for Exploration of Molecular Features and Response to Anti-cancer Drugs. J Mol Biol. 2022 Jun 15;434(11):167528.
Fulltext (DOI)
Pubmed
View record in Web of Science®
III. Petrov I., Alexeyenko A. Individualized discovery of rare cancer drivers in global network context. eLife. 2022;11:e74010.
Fulltext (DOI)
Pubmed
View record in Web of Science®
IV. Petrov I., Alexeyenko A. Comparative performance of network versions, algorithms, and topological properties while discovering novel disease genes. [Manuscript]
Institution: Karolinska Institutet
Supervisor: Alekseenko, Andrey
Co-supervisor: Aurell, Erik; Ernberg, Ingemar
Issue date: 2023-02-27
Rights:
Publication year: 2023
ISBN: 978-91-8016-947-9
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