4.7 Article Proceedings Paper

Integration of molecular network data reconstructs Gene Ontology

期刊

BIOINFORMATICS
卷 30, 期 17, 页码 I594-I600

出版社

OXFORD UNIV PRESS
DOI: 10.1093/bioinformatics/btu470

关键词

-

资金

  1. European Research Council (ERC) [278212]
  2. National Science Foundation (NSF) Cyber-Enabled Discovery and Innovation (CDI) [OIA-1028394]
  3. Serbian Ministry of Education and Science [III44006]
  4. ARRS [J1-5454]
  5. Office Of The Director
  6. Office of Integrative Activities [1028394] Funding Source: National Science Foundation

向作者/读者索取更多资源

Motivation: Recently, a shift was made from using Gene Ontology (GO) to evaluate molecular network data to using these data to construct and evaluate GO. Dutkowski et al. provide the first evidence that a large part of GO can be reconstructed solely from topologies of molecular networks. Motivated by this work, we develop a novel data integration framework that integrates multiple types of molecular network data to reconstruct and update GO. We ask how much of GO can be recovered by integrating various molecular interaction data. Results: We introduce a computational framework for integration of various biological networks using penalized non-negative matrix tri-factorization (PNMTF). It takes all network data in a matrix form and performs simultaneous clustering of genes and GO terms, inducing new relations between genes and GO terms (annotations) and between GO terms themselves. To improve the accuracy of our predicted relations, we extend the integration methodology to include additional topological information represented as the similarity in wiring around non-interacting genes. Surprisingly, by integrating topologies of bakers' yeasts protein-protein interaction, genetic interaction (GI) and co-expression networks, our method reports as related 96% of GO terms that are directly related in GO. The inclusion of the wiring similarity of non-interacting genes contributes 6% to this large GO term association capture. Furthermore, we use our method to infer new relationships between GO terms solely from the topologies of these networks and validate 44% of our predictions in the literature. In addition, our integration method reproduces 48% of cellular component, 41% of molecular function and 41% of biological process GO terms, outperforming the previous method in the former two domains of GO. Finally, we predict new GO annotations of yeast genes and validate our predictions through GIs profiling.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Biochemical Research Methods

Fuse: multiple network alignment via data fusion

Vladimir Gligorijevic, Noel Malod-Dognin, Natasa Przulj

BIOINFORMATICS (2016)

Review Biochemical Research Methods

Integrative methods for analyzing big data in precision medicine

Vladimir Gligorijevic, Noel Malod-Dognin, Natasa Przulj

PROTEOMICS (2016)

Editorial Material Multidisciplinary Sciences

Network analytics in the age of big data

Natasa Przulj, Noel Malod-Dognin

SCIENCE (2016)

Article Multidisciplinary Sciences

A global genetic interaction network maps a wiring diagram of cellular function

Michael Costanzo, Benjamin VanderSluis, Elizabeth N. Koch, Anastasia Baryshnikova, Carles Pons, Guihong Tan, Wen Wang, Matej Usaj, Julia Hanchard, Susan D. Lee, Vicent Pelechano, Erin B. Styles, Maximilian Billmann, Jolanda van Leeuwen, Nydia van Dyk, Zhen-Yuan Lin, Elena Kuzmin, Justin Nelson, Jeff S. Piotrowski, Tharan Srikumar, Sondra Bahr, Yiqun Chen, Raamesh Deshpande, Christoph F. Kurat, Sheena C. Li, Zhijian Li, Mojca Mattiazzi Usaj, Hiroki Okada, Natasha Pascoe, Bryan-Joseph San Luis, Sara Sharifpoor, Emira Shuteriqi, Scott W. Simpkins, Jamie Snider, Harsha Garadi Suresh, Yizhao Tan, Hongwei Zhu, Noel Malod-Dognin, Vuk Janjic, Natasa Przulj, Olga G. Troyanskaya, Igor Stagljar, Tian Xia, Yoshikazu Ohya, Anne-Claude Gingras, Brian Raught, Michael Boutros, Lars M. Steinmetz, Claire L. Moore, Adam P. Rosebrock, Amy A. Caudy, Chad L. Myers, Brenda Andrews, Charles Boone

SCIENCE (2016)

Article Biochemistry & Molecular Biology

Systematic protein-protein interaction mapping for clinically relevant human GPCRs

Kate Sokolina, Saranya Kittanakom, Jamie Snider, Max Kotlyar, Pascal Maurice, Jorge Gandia, Abla Benleulmi-Chaachoua, Kenjiro Tadagaki, Atsuro Oishi, Victoria Wong, Ramy H. Malty, Viktor Deineko, Hiroyuki Aoki, Shahreen Amin, Zhong Yao, Xavier Morato, David Otasek, Hiroyuki Kobayashi, Javier Menendez, Daniel Auerbach, Stephane Angers, Natasa Przulj, Michel Bouvier, Mohan Babu, Francisco Ciruela, Ralf Jockers, Igor Jurisica, Igor Stagljar

MOLECULAR SYSTEMS BIOLOGY (2017)

Article Multidisciplinary Sciences

Graphlet-based Characterization of Directed Networks

Anida Sarajlic, Noel Malod-Dognin, Omer Nebil Yaveroglu, Natasa Przulj

SCIENTIFIC REPORTS (2016)

Article Multidisciplinary Sciences

Unified Alignment of Protein-Protein Interaction Networks

Noel Malod-Dognin, Kristina Ban, Natasa Przulj

SCIENTIFIC REPORTS (2017)

Review Pharmacology & Pharmacy

Critical Review on Zeolite Clinoptilolite Safety and Medical Applications in vivo

Sandra Kraljevic Pavelic, Jasmina Simovi Medica, Darko Gumbarevic, Ana Filosevic, Natasa Przulj, Kresimir Pavelic

FRONTIERS IN PHARMACOLOGY (2018)

Article Multidisciplinary Sciences

Towards a data-integrated cell

Noel Malod-Dognin, Julia Petschnigg, Sam F. L. Windels, Janez Povh, Harry Hemmingway, Robin Ketteler, Natasa Przulj

NATURE COMMUNICATIONS (2019)

Article Biochemical Research Methods

Chromatin network markers of leukemia

N. Malod-Dognin, V Pancaldi, A. Valencia, N. Przulj

BIOINFORMATICS (2020)

Article Biochemical Research Methods

Multi-project and Multi-profile joint Non-negative Matrix Factorization for cancer omic datasets

D. A. Salazar, N. Przulj, C. F. Valencia

Summary: This study introduces a novel method capable of integrating multi-omic data from different sources and identifying patient and cell line groups enriched in cancer-associated gene clusters. The method also predicts drug profiles for patients and identifies genetic signatures for tumors resistant and sensitive to specific drugs.

BIOINFORMATICS (2021)

Article Biochemistry & Molecular Biology

Integrated Data Analysis Uncovers New COVID-19 Related Genes and Potential Drug Re-Purposing Candidates

Alexandros Xenos, Noel Malod-Dognin, Carme Zambrana, Natasa Przulj

Summary: To understand COVID-19, researchers used an integrated cell (iCell) concept with three omics networks to study its molecular basis. They compared patient-based and cell line-based iCells and found significant differences, indicating the limitations of using cell lines in studying this disease. By comparing infected and control patient-based iCells, they identified genes whose functioning is altered by the disease. They also predicted drugs for repurposing and confirmed the binding of these drugs to their targets. The study highlights the applicability of the iCell framework for studying human diseases.

INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES (2023)

Article Mathematical & Computational Biology

Omics Data Complementarity Underlines Functional Cross-Communication in Yeast

Noel Malod-Dognin, Natasa Przulj

JOURNAL OF INTEGRATIVE BIOINFORMATICS (2017)

Article Biochemical Research Methods

Rebuttal to the Letter to the Editor in response to the paper: proper evaluation of alignment-free network comparison methods

Omer Nebil Yaveroglu, Noel Malod-Dognin, Tijana Milenkovic, Natasa Przulj

BIOINFORMATICS (2017)

Proceedings Paper Computer Science, Interdisciplinary Applications

PATIENT-SPECIFIC DATA FUSION FOR CANCER STRATIFICATION AND PERSONALISED TREATMENT

Vladimir Gligorijevic, Noel Malod-Dognin, Natasa Przulj

PACIFIC SYMPOSIUM ON BIOCOMPUTING 2016 (2016)

暂无数据