- From: Helena Deus <helenadeus@gmail.com>
- Date: Fri, 24 Feb 2012 17:10:18 +0000
- To: Oliver Ruebenacker <curoli@gmail.com>
- Cc: public-semweb-lifesci <public-semweb-lifesci@w3.org>
- Message-ID: <CAPkJ_9nBqYZJQJ74m1QgKtKHs=QSirDADSvO+CC9YoLnzuGyWQ@mail.gmail.com>
Hi Oliver, Thank you for the paragraph, with your permission I would like to add it to the wiki; and great to hear that you are interested in participating. Best, Lena On Fri, Feb 24, 2012 at 4:55 PM, Oliver Ruebenacker <curoli@gmail.com>wrote: > Hello Helena, All, > > I'm interested in joining the Systems Biology Taskforce. Sorry I > could not make the initial call. My interest is turning biological > knowledge into mathematical models, automatically. A brief description > is below. > > Thanks! > > Take care > Oliver > > Living organisms are so enormously complex that we need computer > simulations to understand the consequences of their vast biochemical > reaction networks. As we uncover an increasing part of these networks, > our established knowledge is increasingly stored in free web databases > and available for query and download in machine-readable formats, > especially in the RDF/OWL-based community standard Biological Pathways > Exchange (BioPAX) [1]. The available data is massive and growing, e.g. > Pathway Commons [2] stores 1,700 pathways, 414 organisms, 440,000 > interactions and 86,000 substances. This data is fully linked with > open controlled terminologies such as gene ontology (e.g. anatomical > features) [3] and other free online databases such as ChEBI > (chemicals) [4], KEGG (genes a.o.) [5], UniProt (proteins) [6] and > PubMed (publications) [7]. > > Automatic use of this knowledge for computer simulations of > biological organisms has been an ongoing challenge [8,9,10]. Now, > Systems Biology Pathway Exchange (SBPAX) [11], a BioPAX extension, > allows the inclusion of quantitative data and systems biology terms, > especially the Systems Biology Ontology (SBO) [12]. SBPAX support has > been implemented by the Virtual Cell [13], Signaling Gateway Molecule > Pages [14] and System for the Analysis of Biochemical Pathways - > Reaction Kinetics (SABIO-RK) [15]. For the first time, a mathematical > model can be automatically built and fully annotated from a pathway of > interest. > > Citations: > > [1] Biological Pathway Exchange (BioPAX), www.biopax.org > [2] Pathway Commons, www.pathwaycommons.org > [3] Gene Ontology (GO), www.geneontology.org/ > [4] Chemical Entities of Biological Interest (ChEBI), > www.ebi.ac.uk/chebi/ > [5] Kyoto Encyclopedia of Genes and Genomes (KEGG), wwww.genome.jp/kegg/ > [6] UniProt, www.uniprot.org > [7] PubMed, www.ncbi.nlm.nih.gov/pubmed/ > [8] Modeling without Borders: Creating and Annotating VCell Models > Using the Web, Michael L. Blinov, Oliver Ruebenacker, James C. Schaff > and Ion I. Moraru, Lecture Notes in Computer Science, 2010, Volume > 6053 (2010). > [9] Using views of Systems Biology Cloud: application for model > building, Oliver Ruebenacker, Michael Blinov, Theory in Biosciences, > Volume 130, Number 1, 45-54 (2010). > [10] Integrating BioPAX pathway knowledge with SBML models, Michael > L Blinov, Oliver Ruebenacker, Ion I Moraru, IET Syst. Biol., 2009, > Vol. 3, Iss. 5, pp. 317-328 (2009). > [11] Systems Biology Pathway Exchange (SBPAX), www.sbpax.org > [12] Systems Biology Ontology, www.ebi.ac.uk/sbo/main/ > [13] Virtual Cell, http://vcell.org > [14] Signaling Gateway Molecule Pages, > www.signaling-gateway.org/molecule/ > [15] System for the Analysis of Biological Pathways – Reaction > Kinetics (SABIO-RK), http://sabio.villa-bosch.de/ > > On Tue, Feb 21, 2012 at 4:32 PM, Helena Deus <helenadeus@gmail.com> wrote: > > Dear All, > > > > Please join me tomorrow for the kick-off telco of the Systems Biology > Task > > Force. Systems Biology is about looking at biological systems from an > > integrated perspective and to use that perspective to understand > disease. We > > will be discussing the general goals, strategy and structure of the task > > force. > > > > Please see http://www.w3.org/wiki/HCLSIG/SysBio for an initial > motivation, > > and description, of what this task will be focused on (with due > flexibility > > according to participants input). > > > > > > * Date of Call: Tuesday February 21, 2012 > > * Time of Call: 11:00am Eastern Daylight Time (EDT) > > * Dial-In #: +1.617.761.6200 (Cambridge, MA) > > * [Note: limited access to European dial in numbers below] > > * Dial-In #: +33.4.26.46.79.03 (Nice, France) > > * Dial-In #: +44.203.318.0479 (Bristol, UK) > > * Participant Access Code: 4257 ("HCLS"). > > * IRC Channel: irc.w3.org port 6665 channel #HCLS > > For instant IRC access: > > see [http://www.w3.org/Project/IRC/ W3C IRC page] for details, or > > see [http://cgi.w3.org/member-bin/irc/irc.cgi Web IRC]), Quick Start: > Click > > on > > [http://www.mibbit.com/chat/?server=irc.w3.org:6665&channel=%23hcls > mibbit] > > > > * Duration: ~1h > > * Convener: Helena > > * Scribe: TBD > > > > Kind regards, > > Helena > > > > -- > Oliver Ruebenacker, Computational Cell Biologist > Virtual Cell (http://vcell.org) > SBPAX: Turning Bio Knowledge into Math Models (http://www.sbpax.org) > http://www.oliver.curiousworld.org > -- Helena F. Deus Post-Doctoral Researcher at DERI/NUIG http://lenadeus.info/
Received on Friday, 24 February 2012 17:11:06 UTC