Difference between revisions of "Bayesian Phylogenetic Analysis"

Revision as of 22:30, 26 December 2005

Overview

Today's exercise will focus on phylogenetic analysis using Bayesian methods. We already discussed Bayesian statistics and Bayesian phylogeny in class, but if you want to refresh your memory, then you can read a brief introduction at the end of this page.

In this exercise we will explore how one can determine and use posterior probability distributions over trees, over clades, and over substitution parameters. We will also touch upon the difference between marginal and joint probability distributions.

Getting started

NEXUS files needed:

primatemitDNA.nexus
neanderthalsmall.nexus
hcvsmall.nexus

You have analyzed (versions of) all these data files previously in this course. We will now use Bayesian phylogenetic analysis to complement what we learned in those analyses.

Start long run for later analysis:

Before we really start with today's exercise, you have to start a run that will take quite long time to finish. The results will be analyzed later today, but since we do not want to sit around waiting for it, we will start it now and discuss the results later. For now you should just issue the commands given below without wondering what they mean. I will explain them later in the exercise.

mb

This starts the program, giving you a prompt ("MrBayes> ") where you can enter commands. The next set of commands will load the data file, specify outgroup, request that the program should not prompt you during the run, specify the model, and start the run:

execute neanderthalsmall.nexus
outgroup PAN6030
set autoclose=yes
lset nst=2 rates=gamma
mcmc ngen=300000 savebrlens=yes

The analysis will run for about 35 minutes. Once you have started the run, you should make sure to minimize the window so it won't get in your way. We will return and analyze the results later.

Posterior probability of trees

In today's exercise we will be using the program "MrBayes" to perform Bayesian phylogenetic analysis. MrBayes is a program that, like PAUP*, can be controlled by giving commands at a command line prompt. In fact, there is a substantial overlap between the commands used to control MrBayes and the PAUP command language. This should be a help when you are trying to understand how to use the program.

However, you may notice that the command editor in MrBayes has fewer features than that in PAUP. For instance, you cannot recall previously issued commands by using the arrow-up button, and you can also not use the arrow-left button to move into a command and edit it. Notice that the command "help" will give you a list of all available commands. Issuing "help command" will give you a more detailed description of the specified command along with current option values. This is similar to how "command ?" works in PAUP.

Before you start the exercise, you should make sure that you are now in one of the un-used shell windows, and that you have cd'ed to today's directory! We will now explore how to find and use the posterior probability distribution over trees.

Start program:

mb

Get a quick overview of available commands:

help

Load your sequences:

execute primatemitDNA.nexus

This file contains mitochondrial DNA sequences from 5 different primates. Note that MrBayes accepts input in nexus format, and that this is the same command that was used to load sequences in PAUP*. In general, you can use many of the PAUP commands in MrBayes also.

Inspect data set:

showmatrix

Define outgroup:

outgroup Gibbon

Specify that program should not prompt you during the run:

set autoclose=yes

Specify your model of sequence evolution:

lset nst=2 rates=gamma

This command is again very much like the corresponding one in PAUP. You are specifying that you want to use a model with two substitution types (nst=2), and this is automatically taken to mean that you want to distinguish between transitions and transversions. Furthermore, rates=gamma means that you want the model to use a gamma distribution to account for different rates at different sites in the sequence.

Start Markov chain Monte Carlo sampling:

mcmc ngen=300000 samplefreq=100 nchains=4 savebrlens=yes

What you are doing here is to use the method known as MCMCMC ("Metropolis-coupled Markov chain Monte Carlo") to empirically determine the posterior probability distribution of trees, branch lengths and substitution parameters. Recall that in the Bayesian framework this is how we learn about parameter values: instead of finding the best point estimates, we typically want to quantify the probability of the entire range of possible values. The run will take about 5 minutes to finish (estimated time to finish is shown in the last column of output).

Let us examine the command in detail. First, nchain=4 means that the MCMCMC sampling uses 4 parallel chains: one "cold" from which sampling takes place, and three "heated" that move around in the parameter space more quickly to find additional peaks in the probability distribution. The options ngen=300000 samplefreq=100 lets the search run for 300,000 steps ("generations") and saves a tree once every 100 rounds (meaning that a total of 3,000 trees will be saved). Usually you would probably want to sample from more generations (at least 1,000,000 or so, but the more the better). As you might have guessed, savebrlens=yes means we want the branch length information saved along with the sampled trees.

When the run starts you will see reports about the progress of the four chains. Each line of output lists the generation number and the log likelihoods of the current tree/parameter combination for each of the four chains. The cold chain is the one enclosed in brackets [], while the heated chains are enclosed in parentheses (). Occasionally the chains will swap so one of the heated chains now becomes cold (and sampling then takes place from this chain).

Have a look at the resulting sample files:

Wait until the run has finished (the output stops and the prompt returns), and then switch to your third shell-window (the one where you are not running MrBayes). Open the parameter sampling file in an nedit window:

nedit primatemitDNA.nexus.p

This file contains one line for each sampled point (you may want to turn off line-wrapping in nedit under the preferences menu). Each row corresponds to a certain sample time (or generation). Each column contains the sampled values of one specific parameter. (The first line contains headings telling what the different columns are.) Note how the values of most parameters change a lot during the initial "burnin" period, before they settle near their most probable values. Now, close the nedit window and have a look at the file containing sampled trees:

nedit primatemitDNA.nexus.t

Tree topology is also a parameter in our model, and exactly like for the other parameters we also get samples from tree-space. One tree is printed per line in the parenthetical format used by most (all?) phylogeny software. Since there are 5 taxa in the present data set, the tree-space consists of only 15 different possible trees. Since we have taken 3000 sample points, there must be many lines containing the same tree topology.

Determine "burn-in":

We now have to determine the "burnin", i.e., the number of sample points we have to exclude from our further analysis. Here we will do that by inspecting the likelihood values of the trees saved by MrBayes.

Recall, that the idea in MCMCMC sampling is to move around in parameter space in such a way that the points will be visited according to their posterior probability (i.e., a region with very high posterior probability will be visited frequently). As mentioned in the lecture it takes a while after starting such a process before the sampling gets "out of the foot-hills and into the mountains" of the distribution, and only after this "burnin" period can the sample points be trusted. Here we will try to establish burnin by looking at the likelihoods of each sample point as recorded in the file primatemitDNA.nexus.p. At first the likelihoods increase rapidly. Eventually the increase in likelihood declines, and the likelihoods converge on a steady value (a "plateau"). The burnin is the initial part before this plateau is reached. Now, plot the lnL value for the entire run file:

mbplot.pl primatemitDNA.nexus.p

(mbplot.pl is a small script that extracts the relevant columns from the .p file and uses gnuplot to produce a plot of how the value changes with generation number.) The plot shows you how the likelihood value (y-axis) increases through the generations (x-axis), to finally reach a plateau. If the lnL increases very rapidly, then you may want to zoom in on the first part of the plot. This can be done by first closing the plot window (pressing the "ENTER" button in the shell window should work), and then running mbplot.pl</pl> with a new set of limits:

mbplot.pl primatemitDNA.nexus.p 0 50000

This will show you the <tt>lnL values from generation 0 to generation 50000. Feel free to use other limits if you want to zoom further in or out. Now, look at the x-axis to determine the number of generations required before the plateau is reached. Note down this number and close the window.

Determine number of sample points to discard:

For the analysis that we will perform below, you have to tell MrBayes how many sample points to discard, not how many generations were required to reach the plateau.You get the number of sample points by dividing the number of generations by 100 (recall that we only sampled once every 100 generations). For instance, a burnin of 6000 generations means that you want to discard the first 60 sample points.

Investigate posterior probability distribution over trees:

Return to the shell window where you have MrBayes running. In the command below you should replace XX with the number of sample points you want to discard (60 for instance, but this depends on the plot you made above).

sumt contype=halfcompat showtreeprobs=yes burnin=XX

(Scroll back so you can see the top of the output when the command is done.) This command gives you a summary of the trees that are in the file you examined manually above. As mentioned, the option burnin=XX tells MrBayes how many sample points to discard before analyzing the data. The option contype=halfcompat requests that a majority rule consensus tree is calculated from the set of trees that are left after discarding the burnin. This consensus is the first tree plotted to the screen. Below the consensus cladogram, a consensus phylogram is plotted. The branch lengths in this have been averaged over the trees in which that branch was present (a particular branch corresponds to a bi-partition of the data, and will typically not be present in every sampled tree). The tree also has "clade credibility" values. We will return to the meaning of these later in today's exercise.

What most interests us right now is the list of trees that is printed after the phylogram. These trees are labeled "Tree 1", "Tree 2", etc, and are sorted according to their posterior probability which is indicated by a lower-case p after the tree number. (The upper-case P gives the cumulated probability of trees shown so far, and is useful for constructing a credible set). This list highlights how Bayesian phylogenetic analysis is different from maximum likelihood: Instead of finding the best tree(s), we now get a full list of how probable any possible tree is. Now, draw a sketch of the tree with the highest posterior probability on a piece of paper so you are sure to remember which one it was. How did the less probable trees differ from the most likely one?

The list of trees and probabilities was printed because of the option showtreeprobs=yes. Note that you probably do not want to issue that command if you have much more than 5 taxa! In that case you could instead inspect the file named primatemitDNA.nexus.trprobs which is now present in the same directory as your other files (this file is automatically produced by the sumt command).

Posterior probability of clades

By now the run you started using Neanderthal sequences at the beginning of today's exercise should be finished. Find the shell window and have a look.

Determine burnin:

Again use the procedure outlined above to determine burnin for this data set. (Move to free shell window first):

mbplot.pl neanderthalsmall.nexus.p

Remember that the number of sample points to discard is found by dividing the number of generations by 100).

Find posterior probability of clades:

sumt contype=halfcompat showtreeprobs=no burnin=XX

(Again remember to put your actual number of samples to discard instead of the XX in the command line above.) Now examine the consensus tree that is plotted to screen: On the branches that are resolved, you will notice that numbers have been plotted. These are clade-credibility values, and are in fact the posterior probability that the clade is real (based on the present data set). These numbers are different from the bootstrap values that we briefly investigated previously and that we will return to later in the course: unlike bootstrap support (which have no clear statistical meaning) these are actual probabilities. Furthermore, they have been found using a full probabilistic model, instead of neighbor joining, and have still finished in a reasonable amount of time. These features make Bayesian phylogeny very useful for assessing hypotheses about monophyly.

Based on your values, how much support does the present data set give to the out-of-Africa hypothesis?

Probability distributions over other parameters

As the last thing today, we will now turn away from the tree topology, and instead examine the other parameters that also form part of the probabilistic model. We will do this using a reduced version of the Hepatitis C virus data set that we have also examined previously. Stay in the shell window where you just performed the analysis of Neanderthal sequences.

Load data set:

execute hcvsmall.nexus

Define site partition:

charset 1stpos=1-.\3
charset 2ndpos=2-.\3
charset 3rdpos=3-.\3
partition bycodon = 3:1stpos,2ndpos,3rdpos
set partition=bycodon
prset ratepr=variable

This is an alternative way of specifying that different sites have different rates. Instead of using a gamma distribution and learning which sites have what rates from the data, we are instead using our prior knowledge about the structure of the genetic code to specify that all 1st positions have the same rate, all 2nd positions have the same rate, and all 3rd positions have the same rate. Specifically, charset 1stpos=1-.\3 means that we define a character set named "1stpos" which includes site 1 in the alignment followed by every third site ("\3", meaning it includes sites 1, 4, 7, 11, ...) until the end of the alignment (here denoted ".").

Specify model:

lset nst=6

This specifies that we want to use a model of the General Time Reversible (GTR) type, where all 6 substitution types have separate rate ratios.

When the lset command was discussed previously, a few issues were glossed over. Importantly, and unlike PAUP, the lset command in MrBayes gives no information about whether nucleotide frequencies are equal or not, and whether they should be estimated from the data or not. In MrBayes this is instead controlled by defining the prior probability of the nucleotide frequencies (the command prset can again be used for this). For instance, a model with equal nucleotide frequencies correspond to having prior probability 1 (one) for the frequency vector (A=0.25, C=0.25, G=0.25, T=0.25), and zero prior probability for the infinitely many other possible vectors. As you will see below, the default prior is not this limited, and the program will therefore estimate the frequencies from the data.

Inspect model details:

showmodel

This command gives you a summary of the current model settings. You will also get a summary of how the prior probabilities of all model parameters are set. You will for instance notice that the nucleotide frequencies (parameter labeled "Statefreq") have a "Dirichlet" prior. We will not go into the grisly details of what exactly the Dirichlet distribution looks like, but merely note that it is a distribution over many variables, and that depending on the exact parameters the distribution can be more or less flat. The Dirichlet distribution is a handy way of specifying the prior probability distribution of nucleotide (or amino acid) frequency vectors. The default statefreq prior in MrBayes is the flat or un-informative prior dirichlet(1,1,1,1).

we will not go into the priors for the remaining parameters in any detail, but you may notice that by default all topologies are taken to be equally likely (a flat prior on trees).

Start MCMC sampling:

mcmc ngen=300000 samplefreq=100 nchains=4 savebrlens=yes

The run will take about 5 minutes to finish.

Determine burnin:

Again use the procedure outlined above to determine burnin for this data set. (Move to free shell window first):

~gorm/projekter/bin/mbplot hcvsmall.nexus.p

Remember that the number of sample points to discard is found by dividing the number of generations by 100).

Compute summary of parameter values:

sump burnin=XX

The sump command works much like the sumt command for the non-tree parameters. First, you get a plot of the lnL (not as nice as when using ~gorm/projekter/bin/mbplot though). Secondly, the posterior probability distribution of each parameter is summarized by giving the mean, variance, median, and 95% credible interval.

Based on the reported posterior means, does it seem that r(C<->G) is different from r(A<->C)?. Here r(C<->G) is the relative substitution rate between C and G. (Note that all substitution parameters are given as relative values, with the GT rate arbitrarily set at a value of 1.00).

Marginal vs. joint distributions:

Strictly speaking the comparison above was not entirely appropriate. We first found the overall distribution of the r(C<->G) parameter and then compared its mean to the mean of the overall distribution of the r(A<->C) parameter. By doing things this way, we are ignoring the possibility that the two parameters might be associated in some way. For instance, one parameter might always be larger than the other in any individual sample, even though the total distributions have a substantial overlap. We should instead be looking at the distribution over both parameters simultaneously. A probability distribution over several parameters simultaneously is called a "joint distribution" over the parameters.

By looking at one parameter at a time, we are summing its probability over all values of the other parameters. This is called the marginal distribution. The figure below illustrates a joint distribution over two parameters, and shows how one can think of the marginal distribution as what you get when you view the joint distribution from the side, so to speak (hence the name "marginal").

Joint vs. marginal distribution.

(Figure from Berry, "Statistics - a Bayesian perspective".)

Examine marginal and joint distributions:

Again find a shell window where MrBayes is not running. In the command below I have arbitrarily set the burnin to 50 in order to save you the hassle of entering the value.

cat hcvsmall.nexus.p | grep -v '^Gen' | gawk '{if (NR > 50) print $6}' > rCG.data

This command takes the parameter file, removes the header line, and for all lines that were sampled after the burnin period it prints the r(C<->G) parameter to the file named "rCG.data". Now extract a few extra interesting columns in a similar manner.

cat hcvsmall.nexus.p | grep -v '^Gen' | gawk '{if (NR > 50) print $9}' > rAC.data
cat hcvsmall.nexus.p | grep -v '^Gen' | gawk '{if (NR > 50) print $14}' > rm1.data
cat hcvsmall.nexus.p | grep -v '^Gen' | gawk '{if (NR > 50) print $15}' > rm2.data
cat hcvsmall.nexus.p | grep -v '^Gen' | gawk '{if (NR > 50) print $16}' > rm3.data

We can now plot some interesting distributions:

histo -w 2 -L"CG":"AC" -m ll rCG.data rAC.data

We here use the histo program to plot the marginal distributions of rCG and rAC (issue the command man histo if you want to learn how to use the histo program). Note that while rAC tends to be larger than rCG, there is still a substantial overlap between the distributions. We therefore need to examine the joint distribution to find the real probability that rAC > rCG.

wc -l rCG.data

This gives us a count of how many points remain in the sample files after having discarded the burnin. Write down the number

paste rAC.data rCG.data | gawk '{if ($1>$2) print $0}' | wc -l

This counts the number of sample points where rAC > rCG. You can now find the probability that rAC > rCG by dividing the last number by the first. Note how examining the joint distribution provides you with information that you could not get from simply comparing the marginal distributions. This very simple procedure can also be performed using spread-sheet programs, and can obviously be used to answer many different questions.

We will finish off today's exercise by making one final plot:

histo -w 0.01 -L"1st":"2nd":"3rd" -m lll rm1.data rm2.data rm3.data

This command plots the relative mutation rates at the first, second, and third codon positions. How does this fit with your knowledge of the structure of the genetic code?

Resources

<A TARGET="_BLANK" HREF="http://morphbank.ebc.uu.se/mrbayes/">MrBayes</A>: Bayesian Inference of Phylogeny.

<A NAME="bayesintro">Introduction to Bayesian phylogenetic analysis</A>

As was the case for likelihood methods, Bayesian analysis is founded on having a probabilistic model of how the observed data is produced. (This means that, for a given set of parameter values, you can compute the probability of any possible data set). You will recall from today's lecture that in Bayesian statistics the goal is to obtain a full probability distribution over all possible parameter values. To find this so-called posterior probability distribution requires combining the likelihood and the prior probability distribution.

The prior probability distribution shows your beliefs about the parameters before seeing any data, while the likelihood shows what the data is telling about the parameters. Specifically, the likelihood of a parameter value is the probability of the observed data given that parameter value. (This is the measure we have previously used to find the maximum likelihood estimate). If the prior probability distribution is flat (i.e., if all possible parameter values have the same prior probability) then the posterior distribution is simply proportional to the likelihood distribution, and the parameter value with the maximum likelihood then also has the maximum posterior probability. However, even in this case, using a Bayesian approach still allows one to interpret the posterior as a probability distribution. If the prior is NOT flat, then it may have a substantial impact on the posterior although this effect will diminish with increasing amounts of data. A prior may be derived from the results of previous experiments. For instance one can use the posterior of one analysis as the prior in a new, independent analysis.

In Bayesian phylogeny the parameters are of the same kind as in maximum likelihood phylogeny. Thus, typical parameters include tree topology, branch lengths, nucleotide frequencies, and substitution model parameters such as for instance the transition/transversion ratio or the gamma shape parameter. (The difference is that while we want to find the best point estimates of parameter values in maximum likelihood, the goal in Bayesian phylogeny is instead to find a full probability distribution over all possible parameter values). The observed data is again usually taken to be the alignment, although it would of course be more reasonable to say that the sequences are what have been observed (and the alignment should then be inferred along with the phylogeny).

@@ Line 6: / Line 6: @@
 ==Getting started==
-* '''Log in to your Unix shell account on "genome".'''
-You will need three shell windows for today's exercise. Two are used for running the phylogeny program "MrBayes". The last one will be used for various analyses of the files that are output by MrBayes.
-* '''Construct todays working directory:'''
-<pre>mkdir bayes
-ls -l
-</pre>
-* '''Change to today's working directory'''
-<pre>cd bayes</pre>
-Make sure that you cd to today's directory in all three shell windows.
 * '''NEXUS files needed:'''
@@ Line 53: / Line 38: @@
 In today's exercise we will be using the program "MrBayes" to perform Bayesian phylogenetic analysis. MrBayes is a program that, like PAUP*, can be controlled by giving commands at a command line prompt. In fact, there is a substantial overlap between the commands used to  control MrBayes and the PAUP command language. This should be a help when you are trying to understand how to use the program.
-However, you may notice that the command editor in MrBayes has fewer features than that in PAUP. For instance, you cannot recall previously issued commands by using the arrow-up button, and you can also not use the arrow-left button to move into a command and edit it. Notice that the command "'''help'''" will give you a list of all available commands. Issuing "'''<tt>help ''command''</tt>'''" will give you a more detailed description of the specified command along with current option values. This is similar to how "'''<tt>''command'' ?</tt>'''" works in  PAUP.
+However, you may notice that the command editor in MrBayes has fewer features than that in PAUP. For instance, you cannot recall previously issued commands by using the arrow-up button, and you can also not use the arrow-left button to move into a command and edit it. Notice that the command "'''<tt>help</tt>'''" will give you a list of all available commands. Issuing "'''<tt>help ''command''</tt>'''" will give you a more detailed description of the specified command along with current option values. This is similar to how "'''<tt>''command'' ?</tt>'''" works in  PAUP.
 Before you start the exercise, you should make sure that you are now in one of the un-used shell windows, and that you have cd'ed to today's directory! We will now explore how to find and use the posterior probability distribution over trees.
@@ Line 95: / Line 80: @@
 What you are doing here is to use the method known as MCMCMC ("Metropolis-coupled Markov chain Monte Carlo") to empirically determine the posterior probability distribution of trees, branch lengths and substitution parameters. Recall that in the
-Bayesian framework this is how we learn about parameter values: instead of finding the best point estimates, we typically want to  quantify the probability of the entire range of possible values. The run will take about 5 minutes to finish (estimated time to finish is shown in the last column of output).
+Bayesian framework this is how we learn about parameter values: instead of finding the best point estimates, we typically want to quantify the probability of the entire range of possible values. The run will take about 5 minutes to finish (estimated time to finish is shown in the last column of output).
 Let us examine the command in detail. First, <tt>nchain=4</tt> means that the MCMCMC sampling uses 4 parallel chains: one "cold" from which sampling takes place, and three "heated" that move around in the parameter space more quickly to find additional peaks in the probability distribution. The options <tt>ngen=300000 samplefreq=100</tt> lets the search run for 300,000 steps ("generations") and saves a tree once every 100 rounds (meaning that a total of 3,000 trees will be saved).
@@ Line 122: / Line 107: @@
 Recall, that the idea in MCMCMC sampling is to move around in parameter space in such a way that the points will be visited according to their posterior probability (i.e., a region with very high posterior probability will be visited frequently). As
-mentioned in the lecture it takes a while after starting such a process before the sampling gets "out of the foot-hills and into the mountains" of the distribution, and only after this "burnin" period can the sample points be trusted. Here we will try to establish burnin by looking at the likelihoods of each sample point as recorded in the file <tt>primatemitDNA.nexus.p</tt>. At first the likelihoods increase rapidly. Eventually the increase in likelihood declines, and the likelihoods converge on a steady value (a "plateau"). The burnin is the initial part before this plateau is reached. Now, plot the <tt>lnL</tt> value for the entire run file:</P>
+mentioned in the lecture it takes a while after starting such a process before the sampling gets "out of the foot-hills and into the mountains" of the distribution, and only after this "burnin" period can the sample points be trusted. Here we will try to establish burnin by looking at the likelihoods of each sample point as recorded in the file <tt>primatemitDNA.nexus.p</tt>. At first the likelihoods increase rapidly. Eventually the increase in likelihood declines, and the likelihoods converge on a steady value (a "plateau"). The burnin is the initial part before this plateau is reached. Now, plot the <tt>lnL</tt> value for the entire run file:
+<pre>mbplot.pl primatemitDNA.nexus.p</pre>
-       <BLOCKQUOTE><pre>~gorm/projekter/bin/mbplot primatemitDNA.nexus.p</pre></BLOCKQUOTE>
+(mbplot.pl is a small script that extracts the relevant columns from the <tt>.p</tt> file and uses gnuplot to produce a plot of how the value changes with generation number.) The plot shows you how the likelihood value (y-axis) increases through the generations (x-axis), to finally reach a plateau. If the lnL increases very rapidly, then you may want to zoom in on the first part of the plot. This can be done by first closing the plot window (pressing the "ENTER" button in the shell window should work), and then running <tt>mbplot.pl</pl> with a new set of limits:
-<P>(~gorm/projekter/bin/mbplot is a small script written by me, that extracts the relevant columns from the .p
+<pre>mbplot.pl primatemitDNA.nexus.p 0 50000</pre>
-file and uses gnuplot to produce a plot of how the value changes with generation number).
-The plot shows you how the likelihood value (y-axis) increases through the generations
-(x-axis), to finally reach a plateau. If the lnL increases very rapidly, then you may want
-to  zoom in on the first part of the plot. This can be done by first closing the  plot
-window (pressing the  "ENTER" button in the shell window should work), and then running
-~gorm/projekter/bin/mbplot with a new set of limits:</P>
-       <BLOCKQUOTE><pre>~gorm/projekter/bin/mbplot primatemitDNA.nexus.p 0 50000</pre></BLOCKQUOTE>
+This will show you the <tt>lnL</tt> values from generation 0 to generation 50000. Feel free to use other limits if you want to zoom further in or out. Now, look at the x-axis to determine the number of generations required before the plateau is reached. Note down this number and close the window.
-<P>This will show you the lnL values from generation 0 to generation 50000. Feel  free
+* '''Determine number of sample points to discard:'''
-to use other limits if you want to zoom further in or out. Now, look at the x-axis to
-determine the number of generations required before the plateau  is reached. Note down
-this number and close the window.</P>
+For the analysis that we will perform below, you have to tell MrBayes how many '''sample points''' to discard, '''not''' how many generations were required to reach the plateau.You get the number of sample points by dividing the number of generations by 100 (recall that we only sampled once every 100 generations). For instance, a burnin of 6000 generations means that you want to discard the first 60 sample points.
-<LI><P><B>Determine number of sample points to discard:</B></P>
+* '''Investigate posterior probability distribution over trees:'''
-<P>For the analysis that we will perform below, you have to tell MrBayes how many
+Return to the shell window where you have MrBayes running. In the command below you should replace XX with the number of sample points you want to discard (60 for instance, but this depends on the plot you made above).
-<B>sample points</B> to discard, <B>not</B> how many generations were required to
-reach the plateau.You get the number of sample points by dividing the number of
-generations by 100 (recall that we only sampled once every 100 generations). For
-instance, a burnin of 6000 generations means that you want to discard the first 60
-sample points.</P>
-<LI><P><B>Investigate posterior probability distribution over trees:</B></P>
-<P>Return to the shell window where you have MrBayes running. In the command below
-you  should replace XX with the number of sample points you want to discard (60 for
-instance, but this depends on the plot you made above).</P>
-<BLOCKQUOTE>
 <pre>sumt contype=halfcompat showtreeprobs=yes burnin=XX</pre>
-</BLOCKQUOTE>
-<P>(Scroll back so you can see the top of the output when the command is done). This
+(Scroll back so you can see the top of the output when the command is done.) This command gives you a summary of the trees that are in the file you  examined manually above. As mentioned, the option <tt>burnin=XX</tt> tells MrBayes how many sample points to discard before analyzing the data. The option <tt>contype=halfcompat</tt> requests that a majority rule consensus tree is calculated from the set of trees that are left after discarding the burnin. This consensus is the first tree plotted  to the screen. Below the consensus cladogram, a consensus phylogram is plotted. The branch lengths in this have been averaged
-command gives you a summary of the trees that are in the file you  examined manually above.
+over the trees in which that branch was present (a particular branch corresponds to a bi-partition of the data, and will typically not be present in every sampled tree). The tree also has "clade credibility" values. We will return to the meaning of these later in today's exercise.
-As mentioned, the option <TT>burnin=XX</TT> tells MrBayes how many sample points to discard
-before analyzing the data. The option <TT>contype=halfcompat</TT> requests that a majority
-rule consensus tree is calculated from the set of trees that are left after discarding the
-burnin. This consensus is the first tree plotted  to the screen. Below the consensus
-cladogram, a consensus phylogram is plotted. The  branch lengths in this have been averaged
-over the trees in which that branch was present (a particular branch corresponds to a
-bi-partition of the data, and will  typically not be present in every sampled tree). The
-tree also has "clade credibility" values. We will return to the meaning of these later in
-today's  exercise.</P>
-<P>What most interests us right now is the list of trees that is printed after the
+What most interests us right now is the list of trees that is printed after the phylogram. These trees are labeled "Tree 1", "Tree 2", etc, and are sorted according to their posterior probability which is indicated by a lower-case p after the tree
-phylogram. These trees are labeled "Tree 1", "Tree 2", etc, and are sorted according
+number. (The upper-case P gives the cumulated probability of trees shown so far, and is useful for constructing a credible set). This list highlights how Bayesian phylogenetic analysis is different from maximum likelihood: Instead of finding the
-to their posterior probability which is indicated by a lower-case p after the tree
+best tree(s), we now get a full list of how probable ''any'' possible tree is. Now, draw a sketch of the tree with the highest posterior probability on a piece of paper so you  are sure to remember which one it was. How did the less probable trees differ
-number. (The  upper-case P gives the cumulated probability of trees shown so far, and
+from the most likely one?
-is useful for  constructing a credible set). This list highlights how Bayesian
-phylogenetic analysis is different from maximum likelihood: Instead of finding the
-best tree(s), we now get a full list of how probable <I>any</I> possible tree is. Now,
-draw a sketch of the tree with the highest posterior probability on a piece of paper
-so you  are sure to remember which one it was. How did the less probable trees differ
-from the most likely one?</P>
-<P>The list of trees and probabilities was printed because of the  option
+The list of trees and probabilities was printed because of the option <tt>showtreeprobs=yes</tt>. Note that you probably do not want to issue that command if you have much more than 5 taxa! In that case you could instead inspect the file named <tt>primatemitDNA.nexus.trprobs</tt> which is now present in the same directory as your other files (this file is automatically produced by the <tt>sumt</tt> command).
-<TT>showtreeprobs=yes</TT>. Note that you probably do not want to  issue that command
-if you have much more than 5 taxa! In that case you could instead inspect the  file
-named <TT>primatemitDNA.nexus.trprobs</TT> which is now present in the same directory
-as your other files (this file is automatically produced by the <TT>sumt</TT>
-command).</P>
-</OL>
+==Posterior probability of clades==
+By now the run you started using Neanderthal sequences at the beginning of today's exercise should be finished. Find the shell window and have a look.
-<P><HR></P>
+* '''Determine burnin:'''
-<H3>Posterior probability of clades</H3>
+Again use the procedure outlined above to determine burnin for this data set. (Move to free shell window first):
+<pre>mbplot.pl neanderthalsmall.nexus.p</pre>
-<P>By now the run you started using Neanderthal sequences at the beginning of today's
+Remember that the number of sample points to discard is found by dividing the number of generations by 100).
-exercise should be finished. Find the shell window and have a look.</P>
-<OL>
+* '''Find posterior probability of clades:'''
-<LI><P><B>Determine burnin:</B></P>
-<P>Again use the procedure outlined above to determine burnin for this data set.  (Move to
-free shell window first):</P>
-<BLOCKQUOTE><pre>~gorm/projekter/bin/mbplot neanderthalsmall.nexus.p</pre></BLOCKQUOTE>
-<P>Remember that the number of sample points to discard is found by dividing the number of
-generations by 100).</P>
-<LI><P><B>Find posterior probability of clades:</B></P>
-<BLOCKQUOTE>
 <pre>sumt contype=halfcompat showtreeprobs=no burnin=XX</pre>
-</BLOCKQUOTE>
-<P>(Again remember to put your actual number of samples to discard instead of the XX in the
-command line above). Now examine the consensus tree that is plotted to screen:  On the
-branches that are resolved, you will notice that numbers have been plotted.  These are
-clade-credibility values, and are in fact the posterior probability that the clade is real
-(based on the present data set). These numbers are different from the bootstrap  values
-that we briefly investigated previously and that we will return to later in the course:
-unlike bootstrap support (which have no clear statistical meaning) these are actual
-probabilities. Furthermore, they have been found using a full probabilistic  model, instead
-of neighbor joining, and have still finished in a reasonable amount of time. These
-features make Bayesian phylogeny very useful for assessing  hypotheses about monophyly.</P>
-<P> Based on your values, how much support does the present data set give to the
-out-of-Africa hypothesis?</P>
-</OL>
-<P><HR></P>
+(Again remember to put your actual number of samples to discard instead of the XX in the command line above.) Now examine the consensus tree that is plotted to screen: On the branches that are resolved, you will notice that numbers have been plotted.  These are clade-credibility values, and are in fact the posterior probability that the clade is real (based on the present data set). These numbers are different from the bootstrap values that we briefly investigated previously and that we will return to later in the course: unlike bootstrap support (which have no clear statistical meaning) these are actual probabilities. Furthermore, they have been found using a full probabilistic  model, instead of neighbor joining, and have still finished in a reasonable amount of time. These features make Bayesian phylogeny very useful for assessing hypotheses about monophyly.
-<H3>Probability distributions over other parameters</H3>
+Based on your values, how much support does the present data set give to the out-of-Africa hypothesis?
-<P>As the last thing today, we will now turn away from the tree topology, and instead
+==Probability distributions over other parameters==
-examine the other parameters that also form part of the probabilistic model. We will do
-this  using a reduced  version of the Hepatitis C virus data set that we have also examined
-previously. Stay in the shell window where you just performed the analysis of Neanderthal
-sequences.</P>
-<OL>
+As the last thing today, we will now turn away from the tree topology, and instead examine the other parameters that also form part of the probabilistic model. We will do this using a reduced version of the Hepatitis C virus data set that we have also examined previously. Stay in the shell window where you just performed the analysis of Neanderthal sequences.
-<LI><P><B>Load data set:</B></P>
+* '''Load data set:'''
-<BLOCKQUOTE>
 <pre>execute hcvsmall.nexus</pre>
-</BLOCKQUOTE>
-<LI><P><B>Define site partition:</B></P>
+* '''Define site partition:'''
 <BLOCKQUOTE><pre>

Difference between revisions of "Bayesian Phylogenetic Analysis"

Revision as of 22:30, 26 December 2005

Contents

Overview

Getting started

Posterior probability of trees

Posterior probability of clades

Probability distributions over other parameters

Joint vs. marginal distribution.

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<A NAME="bayesintro">Introduction to Bayesian phylogenetic analysis</A>

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