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About OMICS Group About OMICS Group OMICS Group is an amalgamation of Open Access publications and worldwide international science conferences and events.

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Presentation on theme: "About OMICS Group About OMICS Group OMICS Group is an amalgamation of Open Access publications and worldwide international science conferences and events."— Presentation transcript:

1 About OMICS Group About OMICS Group OMICS Group is an amalgamation of Open Access publications and worldwide international science conferences and events. Established in the year 2007 with the sole aim of making the information on Sciences and technology ‘Open Access’, OMICS Group publishes 500 online open access scholarly journals in all aspects of Science, Engineering, Management and Technology journals.Open Access publicationsscholarly journals OMICS Group has been instrumental in taking the knowledge on Science & technology to the doorsteps of ordinary men and women. Research Scholars, Students, Libraries, Educational Institutions, Research centers and the industry are main stakeholders that benefitted greatly from this knowledge dissemination. OMICS Group also organizes 500 International conferences annually across the globe, where knowledge transfer takes place through debates, round table discussions, poster presentations, workshops, symposia and exhibitions.International conferences

2 About OMICS International Conferences About OMICS International Conferences OMICS International is a pioneer and leading science event organizer, which publishes around 500 open access journals and conducts over 500 Medical, Clinical, Engineering, Life Sciences, Pharma scientific conferences all over the globe annually with the support of more than 1000 scientific associations and 30,000 editorial board members and 3.5 million followers to its credit. OMICS Group has organized 500 conferences, workshops and national symposiums across the major cities including San Francisco, Las Vegas, San Antonio, Omaha, Orlando, Raleigh, Santa Clara, Chicago, Philadelphia, Baltimore, United Kingdom, Valencia, Dubai, Beijing, Hyderabad, Bengaluru and Mumbai.

3 A new computational approach to graphically highlight regulatory relationships in polymorphic metabolic systems from chromatographic data University of Tunis El Manar Tunis, Tunisia Metabolic network analysis Highlighting regulation laws Understanding Polymorphism origins Simplex computational approach 1 2 3 4 International Conference in Integrative Biology, Valencia, 2015 Nabil SEMMAR

4 Regulation levels (How much?) Scales (where?) Time-dependent systems (when?) Directions (How?) Biosystems (why?)

5 Growth Polymorphism Time-dependent system Acceleration Slow-down Cyclic, rythmic processes Multi-scale system Individual Family Pair Society Feedbacks Ressources Regulation & distribution Binary system Multidirectional system (50%) (10%) (40%) interactive

6 Computational approach to graphically highlight metabolic regulations in polymorphic chromatographic system Polymorphism chromatographic data Polymorphic Background Highlighted relationships Governing processes of polymorphism Input data Output graphics Combinatorial computations Population backbone Metabolic Regulatory Central

7 Illustrative case of the computational approach

8 Analysis of metabolic variations of dopamine derivatives in Parkinson-suffering population Administrated L-dopa (50- 500mg) Dynamic analysis Metabolomics analysis 2) 1)

9 Highlighting metabolic polymorphism by correspondance analysis (CA) and hierarchical cluster analysis (HCA) CA Identify metabolic trends showing relatively high regulations for some metabolites Metabotypes CA

10 Metabolomics Analysis Variability analysis of the 248 metabolic profiles Relative levels

11 Highlighting metabolic polymorphism by correspondance analysis (CA) and hierarchical cluster analysis (HCA) CA Identify metabolic trends showing relatively high regulations for some metabolites Metabotypes Classification of the 248 profiles into appropriate metabotypes Cluster analysis CA

12 1 2 3 4 4 clusters  4 Metabolic trends  4 metabotypes MbTp 1 MbTp 2 MbTp 3 MbTp 4

13

14 Population Metabolic Backbone Polymorphic Background Metabolite x Metabolite y Metabolite z Metabolite x

15 Schéffé’s mixture design M=286 mixtures of n=10 metabolic profiles belonging to 4 metabotypes 1 2 M=286 : : : : : Population stratification into q metabotypes a priori mixture q=4 components Metabotype 1 Metabotype 2 Metabotype 3 Metabotype 4 n 1 + n 2 + n 3 + n 4 = n = 10 individuals

16 Geometrical representation of M mixtures of Schéffé’s design: (10,0,0,0) (0,0,10,0) (0,0,0,10) (9,1,0,0) (8,2,0,0) (7,3,0,0) (6,4,0,0) (5,5,0,0) (4,6,0,0) (3,7,0,0) (2,8,0,0) (1,9,0,0) (0,10,0,0) (9,0,1,0) (8,0,2,0) (7,0,3,0) (6,0,4,0) (5,0,5,0) (4,0,6,0) (3,0,7,0) (2,0,8,0) (1,0,9,0) M = 286 mixture points 286 ways to carry out mixtures of 10 individuals from 4 groups (4,5,1,0) q = 4 components to be combined & n = 10 individuals per mixture Simplex space with (q-1)=3 dimensions

17 Scheffé’s mixture design Response matrix 10 M=286 mixtures of 10 individuals belonging to 4 metabotypes 286 average profiles ++ + + ++ + ++ Average profile (3, 4, 2, 1) Average of 10 individual profiles Metabotypes’ weights Mixtures s

18 ... k =50 1... 1 50 iterations of Scheffé’s design 50 iterations of response matrix Final matrix of 286 smoothed average profiles (a) (b) (c) Metabotypes’ weights Mixtures s (d) Graphical analysis of smoothed results

19 Scatter plots Experimental data Smoothed data Spearman Correlations

20

21 Projections of metabotypes’ weights in the differents (286) mixture points Each point has 4 coordinates   each point results from weighted contributions of the 4 metabotypes

22 Multidirectional relationship between HVA and L-Dopa

23 1 248 : : : : : : :

24 Anti-clockwise Hysteretic relationship between HVA (derivative) and Dopac (precursor) 3-dimensions plot 2-dimensions plot HVA vs Dopac vs Time HVA vs Dopac (implicit time) Anti-clockwise hysteresis

25 … … … … … Lagged regulation Enzyme competitions

26 CONCLUSION

27 3 groups 4 groups Etc. Extraction of multidirectional and multiscale phenotype- dependent relationships Highly noised data treatment Polymorphic system time dependent processes Simplex analysis Highlighting deep regulatory dynamical lows through a serial of static relationships analyzed along time axis Combination, Iteration, Smoothing Multiscale processes Nonlinear Dynamics

28 2007 2010 2011 2013 2014

29 Let Us Meet Again We welcome you all to our future conferences of OMICS International Please Visit: http://integrativebiology.conferenceseries.co m/ http://integrativebiology.conferenceseries.co m/ http://integrativebiology.conferenceseries.co m/ http://conferenceseries.com/ http://www.conferenceseries.com/genetics- and-molecular-biology-conferences.php http://www.conferenceseries.com/genetics- and-molecular-biology-conferences.phphttp://www.conferenceseries.com/genetics- and-molecular-biology-conferences.phphttp://www.conferenceseries.com/genetics- and-molecular-biology-conferences.php


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