Reference no: EM13499939

At the conclusion of this programming assignment, participants should be able to:

- Implement pointers and/or arrays

- Apply parallel arrays

- Compare and contrast pointers and arrays

- Pass output parameters to functions

- Apply repetition structures within algorithms

- Compose C programs consisting of sequential, conditional, and iterative statements

- Create structure charts for a given problem

- Determine an appropriate functional decomposition or top-down design from a structure chart

II. Prerequisites:

Before starting this programming assignment, participants should be able to:

- Analyze a basic set of requirements and apply top-down design principles for a problem

- Apply repetition structures within an algorithm

- Construct while (), for (), or do-while () loops in C

- Compose C programs consisting of sequential, conditional, and iterative statements

- Eliminate redundancy within a program by applying loops and functions

- Create structure charts for a given problem

- Open and close files

- Read, write to, and update files

- Manipulate file handles

- Apply standard library functions: fopen (), fclose (), fscanf (), and fprintf ()

- Compose decision statements ("if" conditional statements)

- Create and utilize compound conditions

- Summarize topics from Hanly&Koffman Chapter 6 including:

o   What is a pointer?

o   What is an output parameter?

III. Overview & Requirements:

DNA is the chemical responsible for carrying instructions that control cells. When the instructions are not recognized by the cells because of mutations, cells do not function properly. Improper functioning of cells can lead to cancer.

If mutations can be identified, then cancer treatments can be applied. Software may be used to identify mutations in the genome. The genome is the collection of DNA instructions in your cells. Most cells contain two sets of chromosomes, one from your father and one from your mother. Each chromosome has billions of DNA strands that consist of nucleotide bases. The four bases are A, C, G, and T. In the double helix structure of DNA, for a normal cell, the A-T and C-G bases are paired.

For this assignment we simplify our model of the genome. Our goal is to identify mutations in a DNA sequence. We will place our normal DNA sequences and "test" sample sequences in a file called "sequences.txt". The section of the file that represents the normal sequences will be identified by a 'N' in the file, and the section that represents the "test" sample sequences will be represented by a 'S'.

Mutations will be identified by mismatched base pairs, such as A-C, A-G, T-C, T-G, C-A, G-A, C-T, and G-T. They will also be identified by changes (flips) in any of the bases from the normal sequence to the sample sequence. Our definition of sequence is base pairs across multiple lines in our file. For example:

N

ATGGAATTCTCGCTC

TACCTTAAGAGCGAG

CGGTCA

GCCAGT

S

TTGGAATTCTAGCTC

AACCTTAAGAGCGCG

CGATGA

GCCACT

The file may contain an unknown number of sequences. However, you may assume that each sequence will not exceed 15 bases as shown above.

Your program must identify each mutation by indicating in which sequence it is found and in which position in the sequence. The results must be written to a file called "mutations.txt". Using the example above, your program would write the following to the file:

Mutation(s) found in sequence 1

Pair 1 flipped pair

Pair 11 mismatched pair

Pair 14 mismatched pair

Mutation(s) found in sequence 2

Pair 3 mismatched pair

Pair 5 flipped pair

BONUS:

Generate randomly paired bases to form random DNA sequences that are written to your "sequences.txt" file.