DN/dS.

Slides:



Advertisements
Similar presentations
IMPRS workshop Comparative Genomics 18 th -21 st of February 2013 Lecture 4 Positive selection.
Advertisements

Phylip PHYLIP (the PHYLogeny Inference Package) is a package of programs for inferring phylogenies (evolutionary trees). PHYLIP is the most widely-distributed.
Quick Lesson on dN/dS Neutral Selection Codon Degeneracy Synonymous vs. Non-synonymous dN/dS ratios Why Selection? The Problem.
GP Applications Two main areas of research Testing genetic programming in areas other techniques have been applied to. Applying genetic programming to.
Maximum Likelihood. Likelihood The likelihood is the probability of the data given the model.
Molecular Evolution Revised 29/12/06
CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Model Selection Anders Gorm Pedersen Molecular Evolution Group Center for Biological Sequence Analysis Technical.
MCB 5472 The Queue, Phylogenetic Reconstruction and Selection Peter Gogarten Office: BSP 404 phone: ,
The gradualist point of view (review) Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages.
MCB 371/372 positive selection 4/25/05 Peter Gogarten Office: BSP 404 phone: ,
The gradualist point of view Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages genes.
The gradualist point of view Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages genes.
MCB 372 Phylogenetic reconstruction Peter Gogarten Office: BSP 404 phone: ,
Other ways to detect positive selection Selective sweeps -> fewer alleles present in population (see contributions from Archaic Humans for example) Repeated.
The gradualist point of view Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages genes.
Ml mapping From: Olga Zhaxybayeva and J Peter Gogarten BMC Genomics 2002, 3:4 Olga Zhaxybayeva and J Peter Gogarten BMC Genomics 2002, 3:4.
Molecular Evolution with an emphasis on substitution rates Gavin JD Smith State Key Laboratory of Emerging Infectious Diseases & Department of Microbiology.
Course overview Tuesday lecture –Those not presenting turn in short review of a paper using the method being discussed Thursday computer lab –Turn in short.
The gradualist point of view Evolution occurs within populations where the fittest organisms have a selective advantage. Over time the advantages genes.
MCB 5472 Types of Selection Peter Gogarten Office: BSP 404 phone: ,
Neutral mutations Neither advantageous nor disadvantageous Invisible to selection (no selection) Frequency subject to ‘drift’ in the population Random.
Positive selection A new allele (mutant) confers some increase in the fitness of the organism Selection acts to favour this allele Also called adaptive.
Trees – what might they mean? Calculating a tree is comparatively easy, figuring out what it might mean is much more difficult. If this is the probable.
MCB 371/372 quartets positive selection 4/20/05 Peter Gogarten Office: BSP 404 phone: ,
Linear and generalised linear models
Adaptive Molecular Evolution Nonsynonymous vs Synonymous.
CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling and molecular phylogeny Anders Gorm Pedersen Molecular Evolution Group Center for Biological.
CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Model Selection Anders Gorm Pedersen Molecular Evolution Group Center for Biological Sequence Analysis Technical.
Maximum Likelihood Molecular Evolution. Maximum Likelihood The likelihood function is the simultaneous density of the observation, as a function of the.
1 HW Clarifications Homology implies shared ancestry Partial sequence identity does not necessarily imply homology A high coverage of sequence identity.
MCB5472 Computer methods in molecular evolution Lecture 4/14/2014.
Input for the Bayesian Phylogenetic Workflow All Input values could be loaded as text file or typing directly. Only for the multifasta file is advised.
In the deterministic model, the time till fixation depends on the selective advantage, but fixation is guaranteed.
Selection versus drift The larger the population the longer it takes for an allele to become fixed. Note: Even though an allele conveys a strong selective.
PAML: Phylogenetic Analysis by Maximum Likelihood Ziheng Yang Depart of Biology University College London
PHYLOGENETICS CONTINUED TESTS BY TUESDAY BECAUSE SOME PROBLEMS WITH SCANTRONS.
Lab3: Bayesian phylogenetic Inference and MCMC Department of Bioinformatics & Biostatistics, SJTU.
Identifying and Modeling Selection Pressure (a review of three papers) Rose Hoberman BioLM seminar Feb 9, 2004.
Molecular Systematics
Estimating evolutionary parameters for Neisseria meningitidis Based on the Czech MLST dataset.
Selectionist view: allele substitution and polymorphism
N=50 s=0.150 replicates s>0 Time till fixation on average: t av = (2/s) ln (2N) generations (also true for mutations with negative “s” ! discuss among.
Paper Review on Cross- species Microarray Comparison Hong Lu
Inferential Statistics Significance Testing Chapter 4.
What is positive selection?
Bayes’ Theorem Reverend Thomas Bayes ( ) Posterior Probability represents the degree to which we believe a given model accurately describes the.
CENTER FOR BIOLOGICAL SEQUENCE ANALYSIS Probabilistic modeling and molecular phylogeny Anders Gorm Pedersen Molecular Evolution Group Center for Biological.
Bayes’ Theorem Reverend Thomas Bayes ( ) Posterior Probability represents the degree to which we believe a given model accurately describes the.
Bootstrap ? See herehere. Maximum Likelihood and Model Choice The maximum Likelihood Ratio Test (LRT) allows to compare two nested models given a dataset.Likelihood.
Neutral mutations Neither advantageous nor disadvantageous Invisible to selection (no selection) Frequency subject to ‘drift’ in the population Mutation.
In populations of finite size, sampling of gametes from the gene pool can cause evolution. Incorporating Genetic Drift.
Modelling evolution Gil McVean Department of Statistics TC A G.
Bayesian II Spring Major Issues in Phylogenetic BI Have we reached convergence? If so, do we have a large enough sample of the posterior?
Phylogenetic reconstruction, probability mapping, types of selection. Peter Gogarten Office: BSP 404 phone: ,
Phylip PHYLIP (the PHYLogeny Inference Package) is a package of programs for inferring phylogenies (evolutionary trees). PHYLIP is the most widely-distributed.
LBA ProtPars. LBA Prot Dist no Gamma and no alignment.
DIVERSIFYING SELECTION AND FUNCTIONAL CONSTRAINT
Neutrality Test First suggested by Kimura (1968) and King and Jukes (1969) Shift to using neutrality as a null hypothesis in positive selection and selection.
Linkage and Linkage Disequilibrium
Pipelines for Computational Analysis (Bioinformatics)
A Brief Introduction of RANSAC
What are the Patterns Of Nucleotide Substitution Within Coding and
Codon based alignments in Seaview
Discrete Event Simulation - 4
CS 581 Tandy Warnow.
Bayesian inference with MrBayes Molecular Phylogenetics – exercise
Phylogenetic reconstruction
Margarita V. Chibalina, Dmitry A. Filatov  Current Biology 
Cancer Evolution: No Room for Negative Selection
Reverend Thomas Bayes ( )
Presentation transcript:

dN/dS

Testing for selection using dN/dS ratio dN/dS ratio (aka Ka/Ks or ω (omega) ratio) where dN = number of non-synonymous substitutions / number of all possible non-synonymous substitutions dS = number of synonymous substitutions / number of all possible synonymous substitutions dN/dS >1 positive, Darwinian selection The synonymous and non-synonymous rates dN and dS are defined as the numbers of synonymous and nonsynonymous substitutions per site. The ratio of the two rates omega=dN/dS then measures selective pressure at the protein level. If selection level has no effect on fitness, nonsynonymous mutations will be fixed at the same rate as synonymous mutations so that dN=dS and omega=1. If nonsynonymous mutations are deleterious purifying selection will reduce their fixation rate so that dN<dS and omega<1. If nonsynonymous mutations are favored by Darwinian selection, they will be fixed at a higher rate than synonymous mutations resulting in dN>dS and omega>1. dN/dS =1 neutral evolution - THIS IS THE USUAL NULL HYPOTHESIS dN/dS <1 negative, purifying selection - THIS IS TRUE FOR MOST CODONS

PAML (codeml) the basic model Paml is available from the author at http://abacus.gene.ucl.ac.uk/software/paml.html

sites versus branches You can determine omega for the whole dataset; however, usually not all sites in a sequence are under selection all the time. PAML (and other programs) allow to either determine omega for each site over the whole tree, , or determine omega for each branch for the whole sequence, . It would be great to do both, i.e., conclude codon 176 in the vacuolar ATPases was under positive selection during the evolution of modern humans – alas, a single site often does not provide much statistics. PAML does provide a branch site model.

PAML – codeml – sites model (cont.) the program is invoked by typing codeml followed by the name of a control file that tells the program what to do. paml can be used to find the maximum likelihood tree, however, the program is rather slow. Phyml is a better choice to find the tree, which then can be used as a user tree. An example for a codeml.ctl file is codeml.hv1.sites.ctl This file directs codeml to run three different models: one with an omega fixed at 1, a second where each site can be either have an omega between 0 and 1, or an omega of 1, and third a model that uses three omegas as described before for MrBayes. The output is written into a file called Hv1.sites.codeml_out (as directed by the control file). Point out log likelihoods and estimated parameter line (kappa and omegas) Additional useful information is in the rst file generated by the codeml

PAML – codeml – branch model dS -tree dN -tree

where to get help else read the manuals and help files check out the discussion board at https://www.ucl.ac.uk/discussions/viewforum.php?f=54 pal2nal: http://www.bork.embl.de/pal2nal/ else there is a new program on the block called hy-phy (=hypothesis testing using phylogenetics). The easiest is probably to run the analyses on the authors datamonkey.

Illustration of a biased random walk Image generated with Paul Lewis's MCRobot Figure generated using MCRobot program (Paul Lewis, 2001)

sites model in MrBayes The MrBayes block in a nexus file might look something like this: begin mrbayes; set autoclose=yes; lset nst=2 rates=gamma nucmodel=codon omegavar=Ny98; mcmcp samplefreq=500 printfreq=500; mcmc ngen=500000; sump burnin=50; sumt burnin=50; end;

plot LogL to determine which samples to ignore the same after rescaling the y-axis

for each codon calculate the the average probability copy paste formula enter formula plot row

LAGLIDAG motifs are at codon 232-243 and 442-451

FEL Analysis using hyphy on the datamonkey

FEL Analysis using hyphy on the datamonkey