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2014 Language Design and Implementation for Computational Modeling, Simulation and Visualization Vishakha Sharma (PhD Candidate) Adriana Compagnoni (Advisor)

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Presentation on theme: "2014 Language Design and Implementation for Computational Modeling, Simulation and Visualization Vishakha Sharma (PhD Candidate) Adriana Compagnoni (Advisor)"— Presentation transcript:

1 2014 Language Design and Implementation for Computational Modeling, Simulation and Visualization Vishakha Sharma (PhD Candidate) Adriana Compagnoni (Advisor) Department of Computer Science Stevens Institute of Technology, NJ October 8-10, 2014, Phoenix, AZ #GHC14 2014

2 Computational Biology  The convergence of Biology and Computer Science  An emerging discipline  Studies complex biological systems  Large numbers of diverse and multifunctional elements  Selective Interactions  It combines experimental and computational research  Intrinsically interdisciplinary  Accelerates our understanding of life.

3 2014 Suitability of Concurrent Programming Languages  Biological processes are intrinsically concurrent  Communication channels can be used to represent biological reactions (send/receive handshake)  Dynamic creation of communication channels enables reactions in a changing system (multiplication, growth, death, mutation,…)

4 2014 Benefits of Computational Models  In vitro vs in silico experiments: In vitro (may be) is faster, but in silico is cheaper  Can venture what is not observable suggesting unforeseen experiments.  Offer a testbed for unknown behavior – what if…  Can generate synthetic data

5 2014 The Cost of Drug Development For companies that have launched more than three drugs, the median cost per new drug is $4.2 billion; for those that have launched more than four, it is $5.3 billion. Even if a company only develops one drug, the median spending is still a hefty $351 million. 98 companies, 220 drugs 8/11/2013 Matthew Herpes, Forbes

6 2014 Computational Model of Antibacterial Surfaces  Goal: Develop biomaterials that minimize bacterial colonization  Proposal: Building Computational Model to reduce number of experiments and predict behavior

7 2014 Motivating Example: Bifunctional Polymer Brushes Dr. Henk J. Busscher’s group at University Medical Center Groningen, The Netherlands

8 2014 BioScape: A High Level Modeling and Simulation Language BioScape Syntax attach@0.00000184, 2.0 kill@0.00001671, 1.0 Bac()@movBac, stepBac, shapeBac() = !attach.PBac() + mov.Bac() PBac()@movPBac, stepPBac, shapePBac() = delay@0.000001.(PBac() | PBac()) + ?kill().DBac() DBac()@movDBac, stepDBac, shapeDBac() = delay@0.1 PEO()@movPEO, stepPEO, shapePEO() = ?attach() Lyso()@movLyso, stepLyso, shapeLyso() = !kill() Adriana Compagnoni, Vishakha Sharma, Yifei Bao, Matthew Libera, Svetlana Sukhishvili. Philippe Bidinger, Livio Bioglio and Eduardo Bonelli. BioScape: A Modeling and Simulation Language for Bacteria-Materials Interactions. Electronic Notes in Theoretical Computer Science, 293(0):35 - 49, 2013. Proceedings of the Third International Workshop on Interactions Between Computer Science and Biology (CS2Bio'12).

9 2014 From Lab Data To Computational Model Three different surfaces ConjugatesSurface coverage by Lysozyme in Wet Lab [%] Number of PEO Binding Sites in silico Number of Lysozyme Binding Sites in silico Pluronic Unmodified 10000 1% Pl-Lys3268003200 100% Pl-Lys4753004700

10 2014 From Lab Data To Computational Model Ten times faster !!!  1 unit of simulation time corresponds to 10 minutes of wet lab.  Adhesion phase: 12 units of simulation time corresponds to 120 minutes or 2 hours of wet lab.  Growth phase: 108 units of simulation time corresponds to 1080 minutes or 18 hours of wet lab. Simulation Time:

11 2014 Simulation Results Vishakha Sharma, Adriana Compagnoni, Matthew Libera, Agnieszka K. Muszanska, Henk J. Busscher, Henny C. van der Mei. Simulating Anti-adhesive and Antibacterial Bifunctional Polymers for Surface Coating using BioScape. In Proceedings of the ACM Conference on Bioinformatics, Computational Biology and Biomedical Informatics (ACM BCB), Washington, DC, September 22 - 25, 2013. Adhesion Phase Growth Phase Training Data Validation Experiment 4: Pluronic Unmodified Experiment 6: 1% Pluronic-Lysozyme Experiment 5: 100% Pluronic-Lysozyme Experiment 1: Pluronic Unmodified Experiment 3: 1% Pluronic-Lysozyme Experiment 2: 100% Pluronic-Lysozyme

12 2014 Predictions of the Computational Model Vishakha Sharma, Adriana Compagnoni, Matthew Libera, Agnieszka K. Muszanska, Henk J. Busscher, Henny C. van der Mei. Simulating Anti-adhesive and Antibacterial Bifunctional Polymers for Surface Coating using BioScape. In Proceedings of the ACM Conference on Bioinformatics, Computational Biology and Biomedical Informatics (ACM BCB), Washington, DC, September 22 - 25, 2013. Between 1% and 10% of conjugation in the initial concentration yields the minimal amount of bacteria with the maximal % of dead bacteria. LESS IS BETTER !!!

13 2014 JAK-STAT Signal Transduction Pathway What do we propose? We propose the construction of a stochastic computational model: for better understanding of cell biology along the pathway, and for the simulation of the effect of existing drugs as well as for development for future treatments. JAK-STAT Signal Transduction Pathway - 46 Reactions

14 2014 Simulation Results COPASI (Deterministic) and SPiM (Stochastic) Population of mRNAc, STAT1c, SOCS1 and STAT1n*-STAT1n* Vishakha Sharma and Adriana Compagnoni. Computational and Mathematical Models of the JAK-STAT Signal Transduction Pathway. In Proceedings of the Summer Computer Simulation Conference (SCSC), Toronto, Canada, July 7 - 10, 2013. Population of mRNA in the cytoplasm mRNAc, using COPASI (red) and SPiM (green and blue)

15 2014 Beyond Biology… (a) Five Component Subsystem of Magellan GPS 315, and (b) Agent-Based Model of Magellan GPS 315 (a) (b) Motivation: Effects of Counterfeit Components in complex multi-component systems. Proposal: Building stochastic computational model for a) identifying counterfeiting and studying its effects in military supply chain; and b) simulation to compare expected failures of a system as a whole versus failure due to the counterfeit components of lesser quality.

16 2014 Simulations Results (a) Failure Counts of Verified and Counterfeit Components for 3 Runs; Run 1 (Black), Run 2 (Blue) and Run 3 (Red) (b) 1 st time stamp – Configuration of assembled systems (ASystem) (c) Last time stamp -Failed assembled systems (FSystem) (a) (b) Stochastic Pi Machine (SPiM) Visual Implementation Vishakha Sharma, Adriana Compagnoni and Jose Emmanuel Ramirez-Marquez. Computational Modeling of the Effects of Counterfeit Components. In Proceedings of the Summer Computer Simulation Conference (SCSC), Monterey, CA, July 6 - 10, 2014. (c)(c)

17 2014 Conclusions and Future Work  We define BioScape, a high-level modeling and simulation language for the stochastic simulation of biological and biomaterials processes.  We visualize biofilm formation.  We construct and validate the stochastic computational model for antibacterial surfaces.  We predict optimal surface configuration with minimal number of attached bacteria and maximal proportion of dead bacteria.  We develop a model that can be used to predict the behavior of the JAK-STAT pathway in the presence of inhibitory agents, creating a platform to assist in the development of new drugs.  We construct a model for identifying counterfeiting and studying its effects in the military supply chain.  Multifunctional coatings – Assembly from first principles  Study adenoviral traffic in healthy/cancerous eukaryotic cells.  Apply our stochastic computational modeling approach to other complex interdisciplinary domains. Future Work: Conclusions:

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