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CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling and molecular phylogeny Anders Gorm Pedersen Molecular Evolution Group Center for Biological.

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1 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling and molecular phylogeny Anders Gorm Pedersen Molecular Evolution Group Center for Biological Sequence Analysis Technical University of Denmark (DTU)

2 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS What is a model? Mathematical models are: IncomprehensibleIncomprehensible UselessUseless No fun at allNo fun at all

3 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS What is a model? Mathematical models are: IncomprehensibleIncomprehensible UselessUseless No fun at allNo fun at all

4 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS What is a model? Model = hypothesis !!!Model = hypothesis !!! Hypothesis (as used in most biological research):Hypothesis (as used in most biological research): –Precisely stated, but qualitative –Allows you to make qualitative predictions Arithmetic model:Arithmetic model: –Mathematically explicit (parameters) –Allows you to make quantitative predictions …

5 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS The Scientific Method Observation of data Model of how system works Prediction(s) about system behavior (simulation)

6 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Modeling: An example

7 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS y = ax + b Simple 2-parameter model Modeling: An example

8 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS y = ax + b Predictions based on Predictions based on model Modeling: An example

9 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Model Fit, parameter estimation y = ax + b Measure of how well the model fits the data: sum of squared errors (SSE) Best parameter estimates: those that give the smallest SSE (least squares model fitting)

10 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Model Fit, parameter estimation y = 1.24x - 0.56 Measure of fit between model and data: sum of squared errors (SSE) Best parameter estimates: those that give the smallest SSE (least squares)

11 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling applied to phylogeny Observed data: multiple alignment of sequencesObserved data: multiple alignment of sequences H.sapiens globinA G G G A T T C A H.sapiens globinA G G G A T T C A M.musculus globinA C G G T T T - A M.musculus globinA C G G T T T - A R.rattus globinA C G G A T T - A R.rattus globinA C G G A T T - A Probabilistic model parameters (simplest case):Probabilistic model parameters (simplest case): –Tree topology and branch lengths –Nucleotide-nucleotide substitution rates (or substitution probabilities) –Nucleotide frequencies:  A,  C,  G,  T

12 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS The maximum likelihood approach I Starting point:Starting point: You have some observed data and a probabilistic model for how the observed data was produced Example:Example: –Data: result of tossing coin 10 times - 7 heads, 3 tails –Model: coin has probability p for heads, 1-p for tails. The probability of observing h heads among n tosses is: Goal:Goal: You want to find the best estimate of the (unknown) parameter value based on the observations. (here the only parameter is “p”) P(h heads) = p h (1-p) n-h hnhn   

13 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS The maximum likelihood approach II  Likelihood = Probability (Data | Model)  Maximum likelihood: Best estimate is the set of parameter values which gives the highest possible likelihood.

14 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Maximum likelihood: coin tossing example Data: result of tossing coin 10 times - 7 heads, 3 tails Model: coin has probability p for heads, 1-p for tails. P(h heads) = p h (1-p) 10-h h 10   

15 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling applied to phylogeny Observed data: multiple alignment of sequencesObserved data: multiple alignment of sequences H.sapiens globinA G G G A T T C A H.sapiens globinA G G G A T T C A M.musculus globinA C G G T T T - A M.musculus globinA C G G T T T - A R.rattus globinA C G G A T T - A R.rattus globinA C G G A T T - A Probabilistic model parameters (simplest case):Probabilistic model parameters (simplest case): –Nucleotide frequencies:  A,  C,  G,  T –Tree topology and branch lengths –Nucleotide-nucleotide substitution rates (or substitution probabilities):

16 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Other models of nucleotide substitution

17 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS More elaborate models of evolution Codon-codon substitution ratesCodon-codon substitution rates (64 x 64 matrix of codon substitution rates) Different mutation rates at different sites in the geneDifferent mutation rates at different sites in the gene (the “gamma-distribution” of mutation rates) Molecular clocksMolecular clocks (same mutation rate on all branches of the tree). Different substitution matrices on different branches of the treeDifferent substitution matrices on different branches of the tree (e.g., strong selection on branch leading to specific group of animals) Etc., etc.Etc., etc.

18 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Computing the probability of one column in an alignment given tree topology and other parameters A C G G A T T C A A C G G T T T - A A A G G A T T - A A G G G T T T - A A A C CA G Columns in alignment contain homologous nucleotides Assume tree topology, branch lengths, and other parameters are given. Assume ancestral states were A and A. Start computation at any internal or external node. Pr =  C P CA (t 1 ) P AC (t 2 ) P AA (t 3 ) P AG (t 4 ) P AA (t 5 ) t4t4 t5t5 t3t3 t1t1 t2t2

19 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Computing the probability of an entire alignment given tree topology and other parameters Probability must be summed over all possible combinations of ancestral nucleotides. (Here we have two internal nodes giving 16 possible combinations) Probability of individual columns are multiplied to give the overall probability of the alignment, i.e., the likelihood of the model. Often the log of the probability is used (log likelihood)

20 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Maximum likelihood phylogeny: heuristic tree search Data:Data: –sequence alignment Model parameters:Model parameters: –nucleotide frequencies, nucleotide substitution rates, tree topology, branch lengths. Choose random initial values for all parameters, compute likelihood Change parameter values slightly in a direction so likelihood improves Repeat until maximum found Results: (1) ML estimate of tree topology (2) ML estimate of branch lengths (3) ML estimate of other model parameters (4) Measure of how well model fits data (likelihood).

21 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Model Selection? y = 1.24x - 0.56 Measure of fit between model and data (e.g., SSE, likelihood, etc.) How do we compare different types of models?

22 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Over-fitting: More parameters always result in a better fit to the data, but not necessarily in a better description y = ax + b 2 parameter model Good description, poor fit y = ax 6 +bx 5 +cx 4 +dx 3 +ex 2 +fx+g 7 parameter model Poor description, good fit

23 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Selecting the best model: the likelihood ratio test The fit of two alternative models can be compared using the ratio of their likelihoods:The fit of two alternative models can be compared using the ratio of their likelihoods: LR =P(Data | M1) = L,M1 P(Data | M2) L,M2 Note that LR > 1 if model 1 has the highest likelihoodNote that LR > 1 if model 1 has the highest likelihood For nested models it can be shown thatFor nested models it can be shown that  = 2*ln(LR) = 2* (lnL,M1 - lnL,M2) follows a  2 distribution with degrees of freedom equal to the number of extra parameters in the most complicated model. This makes it possible to perform stringent statistical tests to determine which model (hypothesis) best describes the data

24 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Asking biological questions in a likelihood ratio testing framework Fit two alternative, nested models to the data.Fit two alternative, nested models to the data. Record optimized likelihood and number of free parameters for each fitted model.Record optimized likelihood and number of free parameters for each fitted model. Test if alternative (parameter-rich) model is significantly better than null-model, given number of additional parameters (n extra ):Test if alternative (parameter-rich) model is significantly better than null-model, given number of additional parameters (n extra ): Compute  = 2 x (lnL Alternative - lnL Null )Compute  = 2 x (lnL Alternative - lnL Null ) Compare  to  2 distribution with n extra degrees of freedomCompare  to  2 distribution with n extra degrees of freedom Depending on models compared, different biological questions can be addressed (presence of molecular clock, presence of positive selection, difference in mutation rates among sites or branches, etc.) Depending on models compared, different biological questions can be addressed (presence of molecular clock, presence of positive selection, difference in mutation rates among sites or branches, etc.)

25 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Likelihood ratio test example: Explosive evolution of bird orders? Bifurcating tree No. branches = 6 No. parameters = 10 lnL = -2034.3 Tree with polytomy No. branches = 5 No. parameters = 9 lnL = -2035.5  = 2 x (lnL Alternative - lnL Null ) = 2 x (-2034.3 - -2035.5) = 2.4 Degrees of freedom = 10 -9 = 1

26 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Likelihood ratio test example: Explosive evolution of bird orders?  = 2 x (lnL Alternative - lnL Null ) = 2.4 Degrees of freedom = 1 Critical value (5% level) = 3.8415 Statistic = 2.4 => 10% < p < 50%  Difference is not significant  No support for internal branch

27 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Likelihood ratio test example: Explosive evolution of bird orders?

28 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Positive selection I: synonymous and non-synonymous mutations 20 amino acids, 61 codons 20 amino acids, 61 codons  –Most amino acids encoded by more than one codon –Not all mutations lead to a change of the encoded amino acid –”Synonymous mutations” are rarely selected against CTA (Leu) CTC (Leu) CTG (Leu) CTT (Leu) CAA (Gln) CCA (Pro) CGA (Arg) ATA (Ile) GTA (Val) TTA (Leu) 1 non-synonymous nucleotide site 1 synonymous nucleotide site 1/3 synonymous 2/3 nonsynymous nucleotide site

29 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Positive selection II: non-synonymous and synonymous mutation rates contain information about selective pressure dN: rate of non-synonymous mutations per non-synonymous sitedN: rate of non-synonymous mutations per non-synonymous site dS: rate of synonymous mutations per synonymous sitedS: rate of synonymous mutations per synonymous site Recall: Evolution is a two-step process:Recall: Evolution is a two-step process: (1) Mutation (random) (2) Selection (non-random) Randomly occurring mutations will lead to dN/dS=1.Randomly occurring mutations will lead to dN/dS=1. Significant deviations from this most likely caused by subsequent selection.Significant deviations from this most likely caused by subsequent selection. dN/dS < 1: Higher rate of synonymous mutations: negative (purifying) selectiondN/dS < 1: Higher rate of synonymous mutations: negative (purifying) selection dN/dS > 1: Higher rate of non-synonymous mutations: positive selectiondN/dS > 1: Higher rate of non-synonymous mutations: positive selection

30 CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Today’s exercise: positive selection in HIV? Fit two alternative models to HIV data:Fit two alternative models to HIV data: –M0: one, common dN/dS ratio in entire sequence –M3: three distinct classes with different dN/dS ratios Use likelihood ratio test to examine if M3 is significantly better than M0,Use likelihood ratio test to examine if M3 is significantly better than M0, If that is the case: is there a class of codons with dN/dS>1 (positive selection)?If that is the case: is there a class of codons with dN/dS>1 (positive selection)? If M3 significantly better than M0 AND if some codons have dN/dS>1 then you have statistical evidence for positive selection.If M3 significantly better than M0 AND if some codons have dN/dS>1 then you have statistical evidence for positive selection. Most likely reason: immune escape (i.e., sites must be in epitopes)Most likely reason: immune escape (i.e., sites must be in epitopes) : Codons showing dN/dS > 1: likely epitopes

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