Integrative pathway enrichment analysis of multivariate omics data

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作者
Marta Paczkowska
Jonathan Barenboim
Nardnisa Sintupisut
Natalie S. Fox
Helen Zhu
Diala Abd-Rabbo
Miles W. Mee
Paul C. Boutros
Jüri Reimand
机构
[1] Ontario Institute for Cancer Research,Computational Biology Program
[2] University of Toronto,Department of Medical Biophysics
[3] University of Toronto,Department of Pharmacology & Toxicology
[4] University of California Los Angeles,Department of Human Genetics
[5] University of California Los Angeles,Department of Urology
[6] University of California Los Angeles,Institute of Precision Health
[7] University of California Los Angeles,Broad Stem Cell Research Centre
[8] University of California Los Angeles,Jonsson Comprehensive Cancer Centre
[9] Wellcome Genome Campus,Wellcome Sanger Institute
[10] The University of Texas MD Anderson Cancer Center,Department of Genomic Medicine
[11] Baylor College of Medicine,Quantitative & Computational Biosciences Graduate Program
[12] University of Toronto,Department of Molecular Genetics
[13] Broad Institute of MIT and Harvard,Department of Medical Oncology
[14] Dana-Farber Cancer Institute,Department of Mathematics
[15] Harvard Medical School,Department of Molecular Medicine (MOMA)
[16] Aarhus University,Laboratory for Medical Science Mathematics
[17] Aarhus University Hospital,Department of Haematology
[18] RIKEN Center for Integrative Medical Sciences,Department for BioMedical Research
[19] RIKEN Center for Integrative Medical Sciences,Department of Medical Oncology
[20] Technical University of Denmark,Graduate School for Cellular and Biomedical Sciences
[21] University of Copenhagen,Department of Genitourinary Medical Oncology—Research, Division of Cancer Medicine
[22] University of Cambridge,Division of Theoretical Bioinformatics
[23] University of Bern,Faculty of Biosciences
[24] Inselspital,Institute for Research in Biomedicine (IRB Barcelona)
[25] University Hospital and University of Bern,Research Program on Biomedical Informatics
[26] University of Bern,Department of Physiology and Biophysics
[27] The University of Texas MD Anderson Cancer Center,Institute for Computational Biomedicine
[28] German Cancer Research Center (DKFZ),Science for Life Laboratory, Department of Cell and Molecular Biology
[29] Heidelberg University,Division of Applied Bioinformatics
[30] University of Texas MD Anderson Cancer Center,Queensland Centre for Medical Genomics, Institute for Molecular Bioscience
[31] Korea Advanced Institute of Science and Technology,CIBIO/InBIO—Research Center in Biodiversity and Genetic Resources
[32] The Barcelona Institute of Science and Technology,Sir Peter MacCallum Department of Oncology
[33] Universitat Pompeu Fabra,Department of Computer Science
[34] Weill Cornell Medicine,Department of Computer Science
[35] Weill Cornell Medicine,Department of Molecular Biophysics and Biochemistry
[36] Uppsala University,Program in Computational Biology and Bioinformatics
[37] German Cancer Research Center (DKFZ),Center for Cancer Research
[38] Barcelona Supercomputing Center,Department of Pathology
[39] The University of Queensland,Bioinformatics Research Centre (BiRC)
[40] Universidade do Porto,CNAG
[41] European Bioinformatics Institute (EMBL-EBI),CRG, Centre for Genomic Regulation (CRG)
[42] University of Milano Bicocca,Biomolecular Engineering Department
[43] Peter MacCallum Cancer Centre,Department of Internal Medicine
[44] The University of Melbourne,Center for Precision Health, School of Biomedical Informatics
[45] Princeton University,The Donnelly Centre
[46] Yale University,Health Data Science Unit
[47] Yale University,Institute of Pharmacy and Molecular Biotechnology and BioQuant
[48] Yale University,Department for Biomedical Research
[49] Massachusetts General Hospital,Computational Biology Center
[50] Massachusetts General Hospital,Department of Biology
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摘要
Multi-omics datasets represent distinct aspects of the central dogma of molecular biology. Such high-dimensional molecular profiles pose challenges to data interpretation and hypothesis generation. ActivePathways is an integrative method that discovers significantly enriched pathways across multiple datasets using statistical data fusion, rationalizes contributing evidence and highlights associated genes. As part of the ICGC/TCGA Pan-Cancer Analysis of Whole Genomes (PCAWG) Consortium, which aggregated whole genome sequencing data from 2658 cancers across 38 tumor types, we integrated genes with coding and non-coding mutations and revealed frequently mutated pathways and additional cancer genes with infrequent mutations. We also analyzed prognostic molecular pathways by integrating genomic and transcriptomic features of 1780 breast cancers and highlighted associations with immune response and anti-apoptotic signaling. Integration of ChIP-seq and RNA-seq data for master regulators of the Hippo pathway across normal human tissues identified processes of tissue regeneration and stem cell regulation. ActivePathways is a versatile method that improves systems-level understanding of cellular organization in health and disease through integration of multiple molecular datasets and pathway annotations.
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