Genome 540 Homework Assignment 1

Due Sunday Jan. 17

Late homework policy is described on course web page.

  1. Download and begin reading Initial sequencing and analysis of the human genome. The Genome International Sequencing Consortium. Nature 409, 860-921 (15 February 2001) . (To print this out, I would recommend the pdf format which corresponds exactly to the printed version, rather than the html format.) For next week, read
  2. Write a program that implements the method described in Lecture 1 to find the longest exactly matching subsequence between two sequences. Specifically, your program should read two input files in "FASTA" format (i.e. having a header line which starts with the character ">" and includes the sequence name, with the sequence itself following on subsequent lines), each of which contains one of the sequences to be compared. As a data check, your program should count the number of bases of each type in each sequence. It should then use the described algorithm to find the longest subsequence present in both sequences. If there are several different perfectly repeated subsequences of the same length, find all of them. When you are looking for these, consider both strands of each sequence (i.e. both the sequence given in the FASTA file, which is sometimes called the 'forward' strand, and its reverse complement, which is sometimes called the 'reverse' strand) simultaneously, so that if the repeated subsequence happens to occur on different strands in the two sequences you will still find it. The easiest way to do this is to create and store in memory a single sequence of length 2N + 2M + 4 (where the two input sequences have lengths N and M bases respectively) constructed by concatenating together the two sequences and their reverse complements (each terminated by a null character to terminate the strings, so that the lexicographic sort does not read across the sequence boundaries), and then create a single list of pointers to each position in this merged sequence, which you then sort.
  3. Using this program, you should then find the longest exactly matching sequences in the Halorhabdus utahensis genome and the Halomicrobium mukohataei genome. Once you find the longest match(es) using your program, you should then try to figure out what biological feature they correspond to. You can do this by exploring the features tables for both organisms here and here.
  4. To test whether your program is working correctly, run it first on the test example indicated below (with two different bacterial genomes) to see whether you get the right answer. You can find the FASTA files for these and other bacterial genomes by going to the NCBI web site and following appropriate links. (On the NCBI site, the FASTA files containing the full genome sequences have the suffix .fna). (To find the biological features, look in the 'Genbank format' files for the organisms (which have the suffix .gbk on the NCBI site) and find the annotated 'feature' in each genome that overlaps the matching segment you found. You don't need to write a program to do this -- just can just read the .gbk file on the web site.)
  5. You must turn in your results and your computer program, using the template (file format) described below. Please put everything into ONE file - do not send an archive of files or a tar file. After creating a plain text file (NOT a word processing document file) in this format, compress it (using either Unix compress, or gzip -- if you don't have access to either of these programs let us know), and send it as an attachment to both Phil at phg@u.washington.edu, and Alan at afrubin@u.washington.edu. The indentation and line breaks below are for readability, and can be omitted. For instance, either of the following is okay:
<result> some text </result> or, <result> some text </result> Here is the template: <gs540_hw assignment='1' name='student name' email='student email'> <results> <result type='first line' file='filename'> first line of one FASTA file </result> <result type='first line' file='filename'> first line of the other FASTA file </result> <result type='nucleotide histogram' file='filename'> Nucleotide histograms should give, for each base or 'ambiguity code' occurring in the sequence, the letter denoting the base, followed by an equals sign, followed by an integer giving the number of times the base occurs in the sequence. Put a comma between the different bases. For instance, A=50,C=50,G=50,T=50,N=2 </result> <result type='nucleotide histogram' file='filename'> A nucleotide histogram for the other fasta file </result> <result type='DNA sequence'> <location file='filename' strand='forward' or 'reverse'> Put the location of the matching subsequence within the input sequence here. The location should be the index of the DNA base in the sequence that is closest to the beginning of the forward strand. Use a coordinate system starting at 1 rather than 0. For example, if the two chromosomal strands are: 5'-ACTGA-3' 3'-TGACT-5' and you found the subsequence TCA on the reverse strand to be the longest match to the other sequence, then the location should be reported as 3. If instead you found CTG on the forward strand, then the location should be reported as 2. </location> <location file='filename' strand='forward' or 'reverse'> Put the location of the matching subsequence in the other input sequence here. </location> longest shared DNA subsequence goes here </result> <result type='DNA sequence'> (give additional matches of same length, if any, in same format as above ... ) </result> </results> <analysis> Put a short identification of the shared DNA subsequence here, for instance: "This DNA sequence is the first 20 bases of an RNA polymerase gene" </analysis> <program> <comments> Any comments about your code or files should go here. </comments> <file name='filename'> file contents here. </file> </program> </gs540_hw> Here is an example of a homework file with the fields filled in with the correct answers for a test case (the program is given only in abbreviated form). <gs540_hw assignment='1' name='Alan Rubin' email='afrubin@u.washington.edu'> <results> <result type='first line' file='NC_000912.fna'> >gi|13507739|ref|NC_000912.1| Mycoplasma pneumoniae M129, complete genome </result> <result type='first line' file='NC_004829.fna'> >gi|31544204|ref|NC_004829.1| Mycoplasma gallisepticum R, complete genome </result> <result type='nucleotide histogram' file='NC_000912.fna'> A=249211,C=162920,T=240560,G=163703 </result> <result type='nucleotide histogram' file='NC_004829.fna'> A=343648,C=156658,T=339399,G=156717 </result> <result type='DNA sequence'> <location file='NC_004829.fna' strand='forward'> 82469 </location> <location file='NC_000912.fna' strand='forward'> 122006 </location> <location file='NC_004829.fna' strand='forward'> 324176 </location> GTCGGGTAAATTCCGTCCCGCTTGAATGGTGTAACCATCTCTTGACTGTCTCGGCTATAG ACTCGGTGAAATCCAGGTACGGGTGAAGACACCCGTTAGGCGCAACGGGACGGAAAGACC CC </result> <result type='DNA sequence'> <location file='NC_004829.fna' strand='reverse'> 82469 </location> <location file='NC_000912.fna' strand='reverse'> 122006 </location> <location file='NC_004829.fna' strand='reverse'> 324176 </location> GGGGTCTTTCCGTCCCGTTGCGCCTAACGGGTGTCTTCACCCGTACCTGGATTTCACCGA GTCTATAGCCGAGACAGTCAAGAGATGGTTACACCATTCAAGCGGGACGGAATTTACCCG AC </result> </results> <analysis> This sequence comes from the 23S ribosomal RNA gene. </analysis> <program> <comments> Run the bash file to compile the C source and run the program. </comments> <file name='hw1.bash'> make ./myprogram seq1.fasta seq2.fasta </file> <file name='makefile'> all: gcc main.c -o myprogram </file> <file name='main.c'> int main() { do_analysis(); return 0; } </file> </program> </gs540_hw>