Code No: 37182

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IV B.Tech I Semester Regular Examinations,Nov/Dec 2009 COMPUTATIONAL MOLECULAR BIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? 1. (a) UPGMA based upon Hamming distances is statistically consistent under the Jukes-Cantor model. Explain.

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(b) UPGMA based upon Jukes-Cantor distances is statistically consistent under the Jukes-Cantor model. Explain. [8+8] 2. Describe the different databases available for storage of protein resources.

[16]

3. Discuss the application of gene chips in various fields of Biotechnology.

[16]

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4. (a) What FASTA programs are available? What are they used for?

(b) What is an E-value? You do a databank search using FASTA with an amino acid sequence as query. The only reported match has an E value of 10. What does this mean for the similarity of two sequences. [8+8]

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5. Write short notes on:

(a) Substitution model in Phylogenetic analysis (b) CLUSTAL W. 6. Explain :

[8+8]

(a) BLAST similarity searching program.

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(b) What type of scoring matrix is used by BLAST? Explain about different substitution matrices? [8+8]

7. How can you analyze the physical properties of proteins.

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8. Discuss in detail how DNA is prapared? ?????

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[16] [16]

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IV B.Tech I Semester Regular Examinations,Nov/Dec 2009 COMPUTATIONAL MOLECULAR BIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ?????

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1. The sequences shown below represent an optimal alignment of the first 50 nucleotides from the human and sheep preproinsulin genes. Estimate the number of substitutions that have occurred in this region. Since humans and sheep last shared a common ancestors using jukes cantor model. Human – ATGGCCCTGT GGATGCCGCCT CCTGCCCCTG CTGGCGCTGC TGGCCCTCTG SHEEP – ATGGCCCTGT GGACACGCCT GGTGCCCCTG CTGGCCCTGC TGGCACTCTG. [16]

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2. Comment on the nature of information provided by structure classification of databases. [16] 3. How could you compare genomes with new template method?

[16]

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4. Who created BLAST and explain the type of scoring matrix used by BLAST? The role of BLAST and in database search tool in molecular biology? [16] 5. How well do threading method work?

[16]

6. (a) Describe how the BLOSUM scoring matrices were constructed. (b) Explain the principle of the Profiles method and its use in multiple sequence alignment. [8+8]

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7. Define the following terms: Expressed sequence tag(EST), positional cloning, Gene prediction, gene expression. Briefly explain each of them. [16] 8. Write short notes on the following : (a) Weighted parsimony

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(b) Unweighted Parsimony.

[8+8] ?????

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Code No: 37182

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IV B.Tech I Semester Regular Examinations,Nov/Dec 2009 COMPUTATIONAL MOLECULAR BIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ?????

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1. What are the chemical forces that stabilize native protein structures? What is the process by which a protein folds from an ensemble of denatured confirmations to a unique native state? [16] 2. What methods would you sue to visually estimate the number of clusters in a gene expression data. [16] 3. Explain:

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(a) Which multiple-sequence alignment method should you use if you want to combine the output of several methods into one single alignment? (b) Which multiple-sequence alignment method should you use if you want to use the structural information associated with some of your sequences? [8+8]

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4. Discuss the properties and assumptions of the JukesCantor and the Kimura 2parameter models DNA evolution. [16] 5. Write short notes on:

(a) Small versus large parsimony

(b) Fitch and Sankoff algorithms.

6. What is protein engineering write about its advantages and disadvantates.

[8+8] [16]

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7. Write a note on:

(a) Pairwise database searching.

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(b) What are Heuristic alignment algorithms? Explain the best known heuristic algorithms BLAST & FASTA? [8+8]

8. Define EST. Describe methodology used the identification of genes. ?????

3

[16]

Code No: 37182

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IV B.Tech I Semester Regular Examinations,Nov/Dec 2009 COMPUTATIONAL MOLECULAR BIOLOGY Bio-Technology Time: 3 hours Max Marks: 80 Answer any FIVE Questions All Questions carry equal marks ????? 1. (a) Maximum likelihood (optimizing parameters under Jukes-Cantor) is statistically consistent under the GTR model. Explain.

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(b) Maximum likelihood (optimizing parameters under the K2P model) is statistically consistent under the Jukes-Cantor model. Explain. [8+8] 2. Distinguish between Distance, Parsimony and maximum likelihood approaches.[16] 3. What is BLAST outline the steps used by BLAST algorithm?

[16]

or

4. What type of scoring matrix is used by FASTA? Explain about different substitution matrices? [16] 5. Name the two most important classification schemes coming under protein structure classification databases. Explain. [16] [16]

7. Describe the organization of nuclear DNA in eukaryotes.

[16]

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6. How the cloning is done? Explain the expression of genes?

8. Justify the statement-“Information of final structure of protein lies in its its primary structures. [16]

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R05 Set No - 1

Explain. [8+8] · 2. Describe the different databases available for storage of protein resources. [16] ... acid sequence as query. The only reported match has an E ...

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