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      Systems medicine disease maps: community-driven comprehensive representation of disease mechanisms

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          Abstract

          The development of computational approaches in systems biology has reached a state of maturity that allows their transition to systems medicine. Despite this progress, intuitive visualisation and context-dependent knowledge representation still present a major bottleneck. In this paper, we describe the Disease Maps Project, an effort towards a community-driven computationally readable comprehensive representation of disease mechanisms. We outline the key principles and the framework required for the success of this initiative, including use of best practices, standards and protocols. We apply a modular approach to ensure efficient sharing and reuse of resources for projects dedicated to specific diseases. Community-wide use of disease maps will accelerate the conduct of biomedical research and lead to new disease ontologies defined from mechanism-based disease endotypes rather than phenotypes.

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          Most cited references42

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          The Systems Biology Graphical Notation.

          Circuit diagrams and Unified Modeling Language diagrams are just two examples of standard visual languages that help accelerate work by promoting regularity, removing ambiguity and enabling software tool support for communication of complex information. Ironically, despite having one of the highest ratios of graphical to textual information, biology still lacks standard graphical notations. The recent deluge of biological knowledge makes addressing this deficit a pressing concern. Toward this goal, we present the Systems Biology Graphical Notation (SBGN), a visual language developed by a community of biochemists, modelers and computer scientists. SBGN consists of three complementary languages: process diagram, entity relationship diagram and activity flow diagram. Together they enable scientists to represent networks of biochemical interactions in a standard, unambiguous way. We believe that SBGN will foster efficient and accurate representation, visualization, storage, exchange and reuse of information on all kinds of biological knowledge, from gene regulation, to metabolism, to cellular signaling.
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            BioPAX – A community standard for pathway data sharing

            BioPAX (Biological Pathway Exchange) is a standard language to represent biological pathways at the molecular and cellular level. Its major use is to facilitate the exchange of pathway data (http://www.biopax.org). Pathway data captures our understanding of biological processes, but its rapid growth necessitates development of databases and computational tools to aid interpretation. However, the current fragmentation of pathway information across many databases with incompatible formats presents barriers to its effective use. BioPAX solves this problem by making pathway data substantially easier to collect, index, interpret and share. BioPAX can represent metabolic and signaling pathways, molecular and genetic interactions and gene regulation networks. BioPAX was created through a community process. Through BioPAX, millions of interactions organized into thousands of pathways across many organisms, from a growing number of sources, are available. Thus, large amounts of pathway data are available in a computable form to support visualization, analysis and biological discovery.
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              Recon3D: A Resource Enabling A Three-Dimensional View of Gene Variation in Human Metabolism

              Genome-scale network reconstructions have helped uncover the molecular basis of metabolism. Here we present Recon3D, a computational resource that includes three-dimensional (3D) metabolite and protein structure data and enables integrated analyses of metabolic functions in humans. We use Recon3D to functionally characterize mutations associated with disease, and identify metabolic response signatures that are caused by exposure to certain drugs. Recon3D represents the most comprehensive human metabolic network model to date, accounting for 3,288 open reading frames (representing 17% of functionally annotated human genes), 13,543 metabolic reactions involving 4,140 unique metabolites, and 12,890 protein structures. These data provide a unique resource for investigating molecular mechanisms of human metabolism. Recon3D is available at http://vmh.life.
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                Author and article information

                Contributors
                amazein@eisbm.org
                rudi.balling@uni.lu
                cauffray@eisbm.org
                Journal
                NPJ Syst Biol Appl
                NPJ Syst Biol Appl
                NPJ Systems Biology and Applications
                Nature Publishing Group UK (London )
                2056-7189
                2 June 2018
                2 June 2018
                2018
                : 4
                : 21
                Affiliations
                [1 ]ISNI 0000 0001 2172 4233, GRID grid.25697.3f, European Institute for Systems Biology and Medicine, CIRI UMR5308, CNRS-ENS-UCBL-INSERM, , Université de Lyon, ; 50 Avenue Tony Garnier, 69007 Lyon, France
                [2 ]ISNI 0000 0001 2295 9843, GRID grid.16008.3f, Luxembourg Centre for Systems Biomedicine (LCSB), , University of Luxembourg, ; Campus Belval, 7 Avenue des Hauts-Fourneaux, L-4362 Esch-sur-Alzette, Luxembourg
                [3 ]ISNI 0000 0004 0639 6384, GRID grid.418596.7, Institut Curie, ; Paris, France
                [4 ]ISNI 0000000121866389, GRID grid.7429.8, INSERM, ; U900 Paris, France
                [5 ]ISNI 0000 0001 2097 6957, GRID grid.58140.38, Mines ParisTech, ; Fontainebleau, France
                [6 ]GRID grid.440907.e, PSL Research University, ; Paris, France
                [7 ]ISNI 0000000105519715, GRID grid.12641.30, Northern Ireland Centre for Stratified Medicine, , Ulster University, ; C-Tric, Altnagelvin Hospital Campus, Derry, Co Londonderry, Northern Ireland, BT47 6SB UK
                [8 ]ISNI 0000 0001 0694 2777, GRID grid.418195.0, The Babraham Institute, ; Babraham Research Campus, Cambridge, CB22 3AT UK
                [9 ]Department of Infection and Immunity, Luxembourg Institute of Health (LIH), House of BioHealth, 29 Rue Henri Koch, L-4354 Esch-Sur-Alzette, Luxembourg
                [10 ]GRID grid.450307.5, Institute for Advanced Biosciences, , University Grenoble-Alpes-INSERM U1209-CNRS UMR5309, ; Site Santé – Allée des Alpes, 38700 La Tronche, France
                [11 ]ISNI 0000 0001 0728 0170, GRID grid.10825.3e, Department of Dermatology and Allergy Center, Odense Research Center for Anaphylaxis, , University of Southern Denmark, ; Odense, Denmark
                [12 ]ISNI 0000 0001 0723 2427, GRID grid.18376.3b, Faculty of Engineering, Computer Engineering Department, , Bilkent University, ; Ankara, 06800 Turkey
                Author information
                http://orcid.org/0000-0001-7137-4171
                http://orcid.org/0000-0001-8086-8915
                http://orcid.org/0000-0002-3671-895X
                http://orcid.org/0000-0003-2657-7361
                http://orcid.org/0000-0002-8562-0975
                http://orcid.org/0000-0003-2724-2002
                http://orcid.org/0000-0002-9517-7284
                http://orcid.org/0000-0003-2226-7411
                Article
                59
                10.1038/s41540-018-0059-y
                5984630
                29872544
                4afcdaa6-d3d8-4975-8708-1e0460457dc5
                © The Author(s) 2018

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 10 January 2018
                : 26 April 2018
                : 4 May 2018
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