1. Fa07CSE 182 CSE182-L4: Database filtering

2. Fa07CSE 182 Summary (through lecture 3) A2 is online We considered the basics of sequence alignment –Opt score computation –Reconstructing alignments –Local alignments –Affine gap costs –Space saving measures The local alignment algorithm (for biological strings) was given by Temple Smith, and Mike Waterman, and is called the Smith-Waterman algorithm (SW) Can we recreate Blast?

3. Fa07CSE 182 The birthday question True or False: 2 people in our class share a birthday? How large should the class be that you can answer this reliably

4. Fa07CSE 182 Basic Probability Q: Toss a coin many times: If it is HEADS, you get a dollar. Otherwise you lose a dollar. What is the money you expect to get (lose) after 100 tosses?

5. Fa07CSE 182 Basic Probability:Expectation Q: Toss a coin many times: If it is HEADS, and the previous time was HEADS too, you get a dollar. Otherwise you lose a dollar. What is the money you expect to get (lose) after 100 tosses?

6. Fa07CSE 182 Blast and local alignment Concatenate all of the database sequences to form one giant sequence. Do local alignment computation with the query.

7. Fa07CSE 182 Large database search Query (m) Database (n) Database size n=100M, Querysize m=1000. O(nm) = 10 11 computations

8. Fa07CSE 182 Why is Blast Fast?

9. Fa07CSE 182 Observations For a typical query, there are only a few ‘real hits’ in the database. Much of the database is random from the query’s perspective Consider a random DNA string of length n. –Pr[A]=Pr[C] = Pr[G]=Pr[T]=0.25 Assume for the moment that the query is all A’s (length m). What is the probability that an exact match to the query can be found?

10. Fa07CSE 182 Basic probability Probability that there is a match starting at a fixed position i = 0.25 m What is the probability that some position i has a match. Dependencies confound probability estimates.

11. Fa07CSE 182 Basic Probability:Expectation Q: Toss a coin many times: If it is HEADS, and the previous time was HEADS too, you get a dollar. Otherwise you lose a dollar. What is the money you expect to get after n tosses? –Let X i be the amount earned in the i-th toss  Total money you expect to earn

12. Fa07CSE 182 Expected number of matches Expected number of matches can still be computed.  Let X i =1 if there is a match starting at position i, X i =0 otherwise  Expected number of matches = i

13. Fa07CSE 182 Expected number of exact Matches is small! Expected number of matches = n*0.25 m –If n=10 7, m=10, Then, expected number of matches = 9.537 –If n=10 7, m=11 expected number of hits = 2.38 –n=10 7,m=12, Expected number of hits = 0.5 < 1 Bottom Line: An exact match to a substring of the query is unlikely just by chance.

14. Fa07CSE 182 Observation 2 What is the pigeonhole principle?  Suppose we are looking for a database string with greater than 90% identity to the query (length 100)  Partition the query into size 10 substrings. At least one much match the database string exactly

15. Fa07CSE 182 Why is this important? Suppose we are looking for sequences that are 80% identical to the query sequence of length 100. Assume that the mismatches are randomly distributed. What is the probability that there is no stretch of 10 bp, where the query and the subject match exactly? Rough calculations show that it is very low. Exact match of a short query substring to a truly similar subject is very high. –The above equation does not take dependencies into account –Reality is better because the matches are not randomly distributed

16. Fa07CSE 182 Just the Facts Consider the set of all substrings of the query string of fixed length W. –Prob. of exact match to a random database string is very low. –Prob. of exact match to a true homolog is very high. –Keyword Search (exact matches) is MUCH faster than sequence alignment

17. Fa07CSE 182 BLAST Consider all (m-W) query words of size W (Default = 11) Scan the database for exact match to all such words For all regions that hit, extend using a dynamic programming alignment. Can be many orders of magnitude faster than SW over the entire string Database (n)

18. Fa07CSE 182 Why is BLAST fast? Assume that keyword searching does not consume any time and that alignment computation the expensive step. Query m=1000, random Db n=10 7, no TP SW = O(nm) = 1000*10 7 = 10 10 computations BLAST, W=11 E(#11-mer hits)= 1000* (1/4) 11 * 10 7 =2384 Number of computations = 2384*100*100=2.384*10 7 Ratio=10 10 /(2.384*10 7 )=420 Further speed improvements are possible

19. Fa07CSE 182 Keyword Matching How fast can we match keywords? Hash table/Db index? What is the size of the hash table, for m=11 Suffix trees? What is the size of the suffix trees? Trie based search. We will do this in class. AATCA 567

20. Fa07CSE 182 Silly Quiz Name a famous Bioinformatics Researcher Name a famous Bioinformatics Researcher who is a woman

21. Fa07CSE 182 Scoring DNA DNA has structure.

22. Fa07CSE 182 DNA scoring matrices So far, we considered a simple match/mismatch criterion. The nucleotides can be grouped into Purines (A,G) and Pyrimidines. Nucleotide substitutions within a group (transitions) are more likely than those across a group (transversions)

23. Fa07CSE 182 Scoring proteins Scoring protein sequence alignments is a much more complex task than scoring DNA –Not all substitutions are equal Problem was first worked on by Pauling and collaborators In the 1970s, Margaret Dayhoff created the first similarity matrices. –“One size does not fit all” –Homologous proteins which are evolutionarily close should be scored differently than proteins that are evolutionarily distant –Different proteins might evolve at different rates and we need to normalize for that

24. Fa07CSE 182 PAM 1 distance Two sequences are 1 PAM apart if they differ in 1 % of the residues. PAM 1 (a,b) = Pr[residue b substitutes residue a, when the sequences are 1 PAM apart] 1% mismatch

25. Fa07CSE 182 PAM1 matrix Align many proteins that are very similar –Is this a problem? 1 PAM evolutionary distance represents the time in which 1% of the residues have changed Estimate the frequency P b|a of residue a being substituted by residue b. PAM1(a,b) = P a|b = Pr(b will mutate to an a after 1 PAM evolutionary distance) Scoring matrix –S(a,b) = log 10 (P ab /P a P b ) = log 10 (P b|a /P b )

26. Fa07CSE 182 PAM 1 Top column shows original, and left column shows replacement residue = PAM1(a,b) = Pr(a|b)

27. Fa07CSE 182 PAM distance Two sequences are 1 PAM apart when they differ in 1% of the residues. When are 2 sequences 2 PAMs apart? 1 PAM 2 PAM

28. Fa07CSE 182 Higher PAMs PAM 2 (a,b) = ∑ c PAM 1 (a,c). PAM 1 (c,b) PAM 2 = PAM 1 * PAM 1 (Matrix multiplication) PAM 250 –= PAM 1 *PAM 249 –= PAM 1 250

29. Fa07CSE 182 Note: This is not the score matrix: What happens as you keep increasing the power?

30. Fa07CSE 182 END of L4