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Schedule for the Afternoon 13:00 – 13:30ChIP-chip lecture 13:30 – 14:30Exercise 14:30 – 14:45Break 14:45 – 15:15Regulatory pathways lecture 15:15 – 15:45Exercise.

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Presentation on theme: "Schedule for the Afternoon 13:00 – 13:30ChIP-chip lecture 13:30 – 14:30Exercise 14:30 – 14:45Break 14:45 – 15:15Regulatory pathways lecture 15:15 – 15:45Exercise."— Presentation transcript:

1 Schedule for the Afternoon 13:00 – 13:30ChIP-chip lecture 13:30 – 14:30Exercise 14:30 – 14:45Break 14:45 – 15:15Regulatory pathways lecture 15:15 – 15:45Exercise (complete previous exercises) 15:45 – 16:00 Wrap up

2 Microarrays for transcription factor binding location analysis (chIP-chip) and the “Active Modules” approach

3 Protein-DNA interactions: ChIP-chip Simon et al., Cell 2001 Lee et al., Science 2002

4 ChIP-chip Microarray Data Differentially represented intergenic regions provides evidence for protein-DNA interaction

5 Network representation of TF-DNA interactions

6 Dynamic role of transcription factors Harbison C, Gordon B, et al. Nature 2004

7 Mapping transcription factor binding sites Harbison C, Gordon B, et al. Nature 2004

8 Integrating gene Expression Data with Interaction Networks

9 Need computational tools able to distill pathways of interest from large molecular interaction databases Data Integration

10 List of Genes Implicated in an Experiment What do we make of such a result? Jelinsky S & Samson LD, Proc. Natl. Acad. Sci. USA Vol. 96, pp. 1486–1491,1999

11 KEGG http://www.genome.jp/kegg/

12 Activated Metabolic Pathways

13 Types of Information to Integrate Data that determine the network (nodes and edges) –protein-protein –protein-DNA, etc… Data that determine the state of the system –mRNA expression data –Protein modifications –Protein levels –Growth phenotype –Dynamics over time

14 Network Perturbations Environmental: –Growth conditions –Drugs –Toxins Genetic: –Gene knockouts –Mutations –Disease states

15 Finding “Active” Sub-graphs Active Modules

16 Finding “Active” Modules/Pathways in a Large Network is Hard Finding the highest scoring subnetwork is NP hard, so we use heuristic search algorithms to identify a collection of high-scoring subnetworks (local optima) Simulated annealing and/or greedy search starting from an initial subnetwork “seed” Considerations: Local topology, sub-network score significance (is score higher than would be expected at random?), multiple states (conditions)

17 Activated Sub-graphs Ideker T, Ozier O, Schwikowski B, Siegel AF. Discovering regulatory and signaling circuits in molecular interaction networks. Bioinformatics. 2002;18 Suppl 1:S233-40.

18 Scoring a Sub-graph Ideker T, Ozier O, Schwikowski B, Siegel AF. Discovering regulatory and signaling circuits in molecular interaction networks. Bioinformatics. 2002;18 Suppl 1:S233-40.

19 Significance Assessment of Active Module Ideker T, Ozier O, Schwikowski B, Siegel AF. Discovering regulatory and signalling circuits in molecular interaction networks. Bioinformatics. 2002;18 Suppl 1:S233-40. Score distributions for the 1st - 5th best scoring modules before (blue) and after (red) randomizing Z- scores (“states”). Randomization disrupts correlation between gene expression and network location.

20 Network Regions of Differential Expression After Gene Deletions Ideker, Ozier, Schwikowski, Siegel. Bioinformatics (2002)

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22 Network based classifier of cancer

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