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BNFO 602, Lecture 2
Usman Roshan
Some of the slides are based upon material by David Wishart of University of Alberta and Ron Shamirof Tel Aviv University
Previously…
• Model of DNA sequence evolution– Poisson model under two state characters– Derivation of expected number of changes on
a single edge of a tree– Jukes-Cantor for four state model (DNA)– Estimating expected number of changes of
two DNA sequences using maximum likelihood
Previously…
• Distance based phylogeny reconstruction methods– UPGMA --- not additive– Neighbor Joining --- additive– Both are fast --- polynomial time– Easy to implement
Previously
• Simulation – Method for simulating evolution of DNA
sequences on a fixed tree– Comparing two different phylogenies for
computing the error rate– Effect of accuracy on real methods as a
function of sequence length, number of sequences, and other factors
Sequencing SuccessesT7 bacteriophagecompleted in 198339,937 bp, 59 coded proteins
Escherichia colicompleted in 19984,639,221 bp, 4293 ORFs
Sacchoromyces cerevisaecompleted in 199612,069,252 bp, 5800 genes
Sequencing SuccessesCaenorhabditis eleganscompleted in 199895,078,296 bp, 19,099 genes
Drosophila melanogastercompleted in 2000116,117,226 bp, 13,601 genes
Homo sapienscompleted in 20033,201,762,515 bp, 31,780 genes
Genomes to Date• 8 vertebrates (human, mouse, rat, fugu, zebrafish)• 3 plants (arabadopsis, rice, poplar)• 2 insects (fruit fly, mosquito)• 2 nematodes (C. elegans, C. briggsae)• 1 sea squirt• 4 parasites (plasmodium, guillardia)• 4 fungi (S. cerevisae, S. pombe)• 200+ bacteria and archebacteria• 2000+ viruses
So what do we do with all this sequence data?
So what do we do with all So what do we do with all this sequence data?this sequence data?
Comparative bioinformatics
DNA Sequence Evolution
AAGACTT -3 mil yrs
-2 mil yrs
-1 mil yrs
today
AAGACTT
T_GACTTAAGGCTT
_GGGCTT TAGACCTT A_CACTT
ACCTT (Cat)
ACACTTC (Lion)
TAGCCCTTA (Monkey)
TAGGCCTT (Human)
GGCTT(Mouse)
T_GACTTAAGGCTT
AAGACTT
_GGGCTT TAGACCTT A_CACTT
AAGGCTT T_GACTT
AAGACTT
TAGGCCTT (Human)
TAGCCCTTA (Monkey)
A_C_CTT (Cat)
A_CACTTC (Lion)
_G_GCTT (Mouse)
_GGGCTT TAGACCTT A_CACTT
AAGGCTT T_GACTT
AAGACTT
Sequence alignments
They tell us about
• Function or activity of a new gene/protein
• Structure or shape of a new protein
• Location or preferred location of a protein
• Stability of a gene or protein
• Origin of a gene or protein
• Origin or phylogeny of an organelle
• Origin or phylogeny of an organism
• And more…
Pairwise alignment
• How to align two sequences?
Pairwise alignment
• How to align two sequences?How to align two sequences?• We use dynamic programming• Treat DNA sequences as strings over the
alphabet {A, C, G, T}
Pairwise alignment
Dynamic programming
Define V(i,j) to be the optimal pairwise alignment score between S1..i and T1..j (|S|=m, |T|=n)
Dynamic programming
Time and space complexity is O(mn)
Define V(i,j) to be the optimal pairwise alignment score between S1..i and T1..j (|S|=m, |T|=n)
Tabular computation of scores
Traceback to get alignment
Local alignment
Finding optimally aligned local regions
Local alignment
Database searching
• Suppose we have a set of 1,000,000 sequences
• You have a query sequence q and want to find the m closest ones in the database---that means 1,000,000 pairwise alignments!
• How to speed up pairwise alignments?
FASTA
• FASTA was the first software for quick searching of a database
• Introduced the idea of searching for k-mers
• Can be done quickly by preprocessing database
FASTA: combine high scoring hits into diagonal runs
BLAST
Key idea: search for k-mers (short matchig substrings) quickly by preprocessing the database.
BLAST
This key idea can also be used for speeding up pairwise alignments when doing multiple sequence alignments
Biologically realistic scoring matrices
• PAM and BLOSUM are most popular
• PAM was developed by Margaret Dayhoff and co-workers in 1978 by examining 1572 mutations between 71 families of closely related proteins
• BLOSUM is more recent and computed from blocks of sequences with sufficient similarity
PAM
• We need to compute the probability transition matrix M which defines the probability of amino acid i converting to j
• Examine a set of closely related sequences which are easy to align---for PAM 1572 mutations between 71 families
• Compute probabilities of change and background probabilities by simple counting
PAM• In this model the unit of evolution is the amount
of evolution that will change 1 in 100 amino acids on the average
The scoring matrix Sab is the ratio of Mab to pb
PAM Mij matrix (x10000)
Multiple sequence alignment
• “Two sequences whisper, multiple sequences shout out loud”---Arthur Lesk
• Computationally very hard---NP-hard
Formally…
Multiple sequence alignment
Unaligned sequences
GGCTT
TAGGCCTT
TAGCCCTTA
ACACTTC
ACTT
Aligned sequences
_G_ _ GCTT_
TAGGCCTT_
TAGCCCTTA
A_ _CACTTC
A_ _C_ CTT_ Conserved regions help us to identify functionality
Sum of pairs score
Sum of pairs score
• What is the sum of pairs score of this alignment?
Tree alignment score
Tree alignment score
Tree Alignment
TAGGCCTT (Human)
TAGCCCTTA (Monkey)
ACCTT (Cat)
ACACTTC (Lion)
GGCTT (Mouse)
Tree Alignment
TAGGCCTT_ (Human)
TAGCCCTTA (Monkey)
A__C_CTT_ (Cat)
A__CACTTC (Lion)
_G__GCTT_ (Mouse)
TAGGCCTT_ A__CACTT_
TGGGGCTT_
AGGGACTT_
0 2
2
11
3
3
2
Tree alignment score = 14
Tree Alignment---depends on tree
TAGGCCTT_ (Human)
TAGCCCTTA (Monkey)
A__C_CTT_ (Cat)
A__CACTTC (Lion)
_G__GCTT_ (Mouse)
TA_CCCTT_ TA_CCCTTA
TA_CCCTT_
TA_CCCTTA
2 3
1
41
0
4
0
Tree alignment score = 15 Switch monkey and cat
Profiles
• Before we see how to construct multiple alignments, how do we align two alignments?
• Idea: summarize an alignment using its profile and align the two profiles
Profile alignment
Iterative alignment(heuristic for sum-of-pairs)
• Pick a random sequence from input set S• Do (n-1) pairwise alignments and align to
closest one t in S• Remove t from S and compute profile of
alignment• While sequences remaining in S
– Do |S| pairwise alignments and align to closest one t
– Remove t from S
Iterative alignment
• Once alignment is computed randomly divide it into two parts
• Compute profile of each sub-alignment and realign the profiles
• If sum-of-pairs of the new alignment is better than the previous then keep, otherwise continue with a different division until specified iteration limit
Progressive alignment
• Idea: perform profile alignments in the order dictated by a tree
• Given a guide-tree do a post-order search and align sequences in that order
• Widely used heuristic
• Can be used for solving tree alignment
Simultaneous alignment and phylogeny reconstruction
• Given unaligned sequences produce both alignment and phylogeny
• Known as the generalized tree alignment problem---MAX-SNP hard
• Iterative improvement heuristic:– Take starting tree– Modify it using say NNI, SPR, or TBR– Compute tree alignment score– If better then select tree otherwise continue until
reached a local minimum
Median alignment
• Idea: iterate over the phylogeny and align every triplet of sequences---takes o(m3) (in general for n sequences it takes O(2nmn) time
• Same profiles can be used as in progressive alignment
• Produces better tree alignment scores (as observed in experiments)
• Iteration continues for a specified limit
Popular alignment programs
• ClustalW: most popular, progressive alignment• MUSCLE: fast and accurate, progressive and
iterative combination• T-COFFEE: slow but accurate, consistency
based alignment (align sequences in multiple alignment to be close to the optimal pairwise alignment)
• PROBCONS: slow but highly accurate, probabilistic consistency progressive based scheme
• DIALIGN: very good for local alignments
MUSCLE
MUSCLE
MUSCLE
Profile sum-of-pairs score
Log expectation score used by MUSCLE
Evaluation of multiple sequence alignments
• Compare to benchmark “true” alignments
• Use simulation
• Measure conservation of an alignment
• Measure accuracy of phylogenetic trees
• How well does it align motifs?
• More…
BAliBASE
• Most popular benchmark of alignments
• Alignments are based upon structure
BAliBASE currently consists of 142 reference alignments, containing over 1000 sequences. Of the 200,000 residues in the database, 58% are defined within the core blocks. The remaining 42% are in ambiguous regions that cannot be reliably aligned. The alignments are divided into four hierarchical reference sets, reference 1 providing the basis for construction of the following sets. Each of the main sets may be further sub-divided into smaller groups, according to sequence length and percent similarity.
BAliBASE
• The sequences included in the database are selected from alignments in either the FSSP or HOMSTRAD structural databases, or from manually constructed structural alignments taken from the literature. When sufficient structures are not available, additional sequences are included from the HSSP database (Schneider et al., 1997). The VAST Web server (Madej, 1995) is used to confirm that the sequences in each alignment are structural neighbours and can be structurally superimposed. Functional sites are identified using the PDBsum database (Laskowski et al., 1997) and the alignments are manually verified and adjusted, in order to ensure that conserved residues are aligned as well as the secondary structure elements.
BAliBASE
• Reference 1 contains alignments of (less than 6) equi-distant sequences, ie. the percent identity between two sequences is within a specified range. All the sequences are of similar length, with no large insertions or extensions. Reference 2 aligns up to three "orphan" sequences (less than 25% identical) from reference 1 with a family of at least 15 closely related sequences. Reference 3 consists of up to 4 sub-groups, with less than 25% residue identity between sequences from different groups. The alignments are constructed by adding homologous family members to the more distantly related sequences in reference 1. Reference 4 is divided into two sub-categories containing alignments of up to 20 sequences including N/C-terminal extensions (up to 400 residues), and insertions (up to 100 residues).
Comparison of alignments on BAliBASE
Parsimonious aligner (PAl)
1. Construct progressive alignment A
2. Construct MP tree T on A
3. Construct progressive alignment A’ on guide-tree T
4. Set A=A’ and go to 3
5. Output alignment and tree with best MP score
PAl
• Faster than iterative improvement• Speed and accuracy both depend upon
progressive alignment and MP heuristic• In practice MUSCLE and TNT are used for
constructing alignments and MP trees• How does PAl compare against traditional
methods?• PAl not designed for aligning structural regions
but focuses on evolutionary conserved regions • Let’s look at performance under simulation
Evaluating alignments under simulation
• We first need a way to evolve sequences with insertions and deletions
• NOTE: evolutionary models we have encountered so far do not account for insertions and deletions
• Not known exactly how to model insertions and deletions
ROSE
• Evolve sequences under an i.i.d. Markov Model• Root sequence: probabilities given by a probability vector
(for proteins default is Dayhoff et. al. values)• Substitutions
– Edge length are integers– Probability matrix M is given as input (default is PAM1*)– For edge of length b probabilty of x y is given by Mb
xy
• Insertion and deletions:– Insertions and deletions follow the same probabilistic model– For each edge probability to insert is iins . – Length of insertion is given by discrete probability distribution
(normally exponential)– For edge of length b this is repeated b times.
• Model tree can be specified as input
Evaluation of alignments
Let’s simulate alignments and
phylogenies and compare them under
simulation!!
Parameters for simulation study
• Model trees: uniform random distribution and uniformly selected random edge lengths
• Model of evolution: PAM with insertions and deletions probabilities selected from a gamma distribution (see ROSE software package)
• Replicate settings: Settings of 50, 100, and 400 taxa, mean sequence lengths of 200 and 500 and avg branch lengths of 10, 25, and 50 were selected. For each setting 10 datasets were produced
Phylogeny accuracy
Alignment accuracy
Running time
Conclusions
• DIALIGN seems to perform best followed by PAl, MUSCLE, and PROBCONS
• DIALIGN, however, is slower than PAl
• Does this mean DIALIGN is the best alignment program?
Conclusions
• DIALIGN seems to perform best followed by PAl, MUSCLE, and PROBCONS
• DIALIGN, however, is slower than PAl• Does this mean DIALIGN is the best
alignment program?• Not necessarily: experiments were
performed under uniform random trees with uniform random edge lengths. Not clear if this emulates the real deal.
Conclusions
• DIALIGN seems to perform best followed DIALIGN seems to perform best followed by PAl, MUSCLE, and PROBCONSby PAl, MUSCLE, and PROBCONS
• DIALIGN, however, is slower than PAlDIALIGN, however, is slower than PAl• Does this mean DIALIGN is the best Does this mean DIALIGN is the best
alignment program?alignment program?• Not necessarily: experiments were Not necessarily: experiments were
performed under uniform random trees performed under uniform random trees with uniform random edge lengths. Not with uniform random edge lengths. Not clear if this emulates the real deal.clear if this emulates the real deal.
• What about sum-of-pairs vs MP scores?
Sum-of-pairs vs MP score
Sum-of-pairs vs MP score
Conclusions
• Optimizing MP scores under this simulation model leads to better phylogenies and alignments
Conclusions
• Optimizing MP scores under this simulation model leads to better phylogenies and alignments
• What other models can we try?
Conclusions
• Optimizing MP scores under this simulation model leads to better phylogenies and alignments
• What other models can we try?• Real data phylogenies as model trees• Birth-death model trees• Other distributions for model trees…• Branch lengths: similar issues…• Evolutionary model parameters estimated
from real data