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An overview of Bioinformatics. Cell and Central Dogma.

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Presentation on theme: "An overview of Bioinformatics. Cell and Central Dogma."— Presentation transcript:

1 An overview of Bioinformatics

2 Cell and Central Dogma

3 Source: “Post-genome Informatics” by M Kanehisa

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5 Deduction and Analogy

6 Biological System (Organism) Reductionistic Synthetic Approach (Experiments) (Bioinformatics) Building Blocks (Genes/Molecules) Source: “Post-genome Informatics” by M Kanehisa

7 Principles Known Physics Chemistry Biology Matter Compound Organism Elementary Elements Genes Particles Yes Yes No Source: “Post-genome Informatics” by M Kanehisa

8 Searching and learning problems in biology Source: “Post-genome Informatics” by M Kanehisa

9 Sequence Comparison: Algorithms and Approaches

10 Homology Search New sequence Similar sequences Expert knowledge Sequence interpretation Sequence database (Primary data) retrieval Source: “Post-genome Informatics” by M Kanehisa

11 Pairwise sequence alignment by dynamic programming Needleman Wunsch alogrithm Source: “Post-genome Informatics” by M Kanehisa

12 Database Search for Similar Sequences

13 Web Lab

14 Motif

15 Source: “Introduction to Protein Structure” by Branden & Tooze

16 Web Lab

17 Motif Search New sequenceExpert knowledge Sequence interpretation Sequence database (Primary data) Motif library (Empirical rules) inference Source: “Post-genome Informatics” by M Kanehisa

18 Introduction to Structural Biology Structural Biology

19 Source: “Introduction to Protein Structure” by Branden & Tooze

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21 Web Lab

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24 Genome Project

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26 Web Lab

27 Genome Sequencing and Genome Annotation

28 A general model of the structure of genomic sequences Source: “Bioinformatics” by D W Mount

29 Microarray

30 Joe Sutliff for Science 291 p1224 (2001) What kind of solution Genomics can provide with ?  High Throughput Gene Discovery

31  165 genes are up-regulated in 75% tumors (MAPK pathway, APC, promotion of mitosis; 69 unknown)  170 genes are down-regulated in 65% tumors (hepatocyte-specific gene products, retinoid metabolism; 75 unknown)  Hierarchical Clustering  K-means  Self Organization Map  Support Vector  Single Value Decomposition

32 Gene Expression andTranscriptome

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35 Web Lab

36 Proteomicsand Functional Genomics

37 Source: “Post-genome Informatics” by M Kanehisa

38 Web Lab

39 Integrative Genomics

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41 Network of physical interactions between nuclear proteins

42 Attributes of generic network structures

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44 Virtual Cell Living Cell Perturbation Environmental change Gene disruption Gene overexpression Dynamic Response Changes in: Gene expression profiles, Etc. Biological Knowledge Molecular and Cellular Biology,Biochemistry, Genetics, etc Basic Principles Practical Applications Complete Genome Sequences Source: “Post-genome Informatics” by M Kanehisa

45 Take Home Message  Define the biological problem.  Why is bioinformatics important ? A synthesis approach.  Prediction is a dangerous game. Always try your best to validate in the bench side.  The devil is in the detail. Always try different bioinformatic tools and databases.  Your knowledge rests on your own practice.

46 Reference Books you will find useful: Bioinformatics -sequence and genome analysis by D W Mount Introduction to Bioinformatics by A M Lesk Post-genome Informatics by M Kanehisa

47 Evolution of molecular biology databases Database category Data contentExamples 1. Literature databaseBibliographic citationsMEDLINE(1971) On-line journals 2. Factual DatabaseNucleic acid sequencesGenBank(1982) Amino acid sequencesEMBL(1982) 3D molecular structuresDDBJ(1984) SWISS_PROT(1986) PDB(1971) 3. Knowledge baseMotif librariesPROSITE(1988) Molecular classificationSCOP(1994) Biochemical pathwaysKEGG(1995)


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