Genome 540 Homework Assignment 1
Due Sunday Jan. 17
Late homework policy is described on course web page.
- 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
- introduction and background (pp. 860-863, up to but not including "Strategic issues")
- the section "Broad genomic landscape" (pp. 875-879, up to but not including "Repeat content of the human genome")
- the section "Gene content of the human genome" (starting p.
892) up to but not including "comparative proteome analysis" (p. 901).
- 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.
- 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.
- 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.)
- 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:
some text
or,
some text
Here is the template:
first line of one FASTA file
first line of the other FASTA file
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
A nucleotide histogram for the other fasta file
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.
Put the location of the matching subsequence in the other input sequence here.
longest shared DNA subsequence goes here
(give additional matches of same length, if any, in same format as above ... )
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"
Any comments about your code or files should
go here.
file contents here.
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).
>gi|13507739|ref|NC_000912.1| Mycoplasma pneumoniae M129, complete genome
>gi|31544204|ref|NC_004829.1| Mycoplasma gallisepticum R, complete genome
A=249211,C=162920,T=240560,G=163703
A=343648,C=156658,T=339399,G=156717
82469
122006
324176
GTCGGGTAAATTCCGTCCCGCTTGAATGGTGTAACCATCTCTTGACTGTCTCGGCTATAG
ACTCGGTGAAATCCAGGTACGGGTGAAGACACCCGTTAGGCGCAACGGGACGGAAAGACC
CC
82469
122006
324176
GGGGTCTTTCCGTCCCGTTGCGCCTAACGGGTGTCTTCACCCGTACCTGGATTTCACCGA
GTCTATAGCCGAGACAGTCAAGAGATGGTTACACCATTCAAGCGGGACGGAATTTACCCG
AC
This sequence comes from the 23S ribosomal RNA gene.
Run the bash file to compile the C source and run the program.
make
./myprogram seq1.fasta seq2.fasta
all:
gcc main.c -o myprogram
int main() {
do_analysis();
return 0;
}