Introduction to phylogenetics using - Google Sites
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Denoting the five species in the original distance matrix by species 1, 2,_ and 5, and using the dij values in the dista
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Introduction to phylogenetics using - Google Sites
Feb 22, 2016 - Three main classes of phylogenetic approaches are introduced, namely distance-based, maximum parsimony, a
Introduction to phylogenetics using Thibaut Jombart
∗
Imperial College London MRC Centre for Outbreak Analysis and Modelling
February 22, 2016
Abstract This practical aims to illustrate the basics of phylogenetic reconstruction using , with an emphasis on how the methods work, how their results can be interpreted, and the relative advantages and limitations of the methods. Three main classes of phylogenetic approaches are introduced, namely distance-based, maximum parsimony, and maximum likelihood methods. We also illustrate how to assess the reliability of individual nodes using bootstrap, and show how a simple linear model can be used to estimate a molecular clock in rooted phylogenies. Methods are illustrated using a )
## ## Converting FASTA alignment into a DNAbin object... ## ## ## Finding the size of a single genome... ## ## ## genome size is: 1,701 nucleotides ## ## ( 30 lines per genome ) ## ## Importing sequences... ## ..................................................................................... ## Forming final object... ## ## ...done. 4
dna ## ## ## ## ## ## ## ## ##
80 DNA sequences in binary format stored in a matrix. All sequences of same length: 1701 Labels: CY013200 CY013781 CY012128 CY013613 CY012160 CY012272 ... Base composition: a c g t 0.335 0.200 0.225 0.239
class(dna) ## [1] "DNAbin" Sequences are stored as DNAbin objects, an efficient representation of DNA/RNA sequences which use bytes (as opposed to character strings) to code nucleotides, resulting in considerable savings in terms of memory required to store the ) class(D) ## [1] "dist" length(D) ## [1] 3160 D is an object of class dist which contains the distances between every pairs of sequences. Now that genetic distances between isolates have been computed, we need to visualize this information. There are n(n − 1)/2 distances for n sequences; here, n = 80 so that the genetic relationships between the sampled isolates are described by 80 × 79/2 = 3160 pairwise distances. Most of the time, summarising such information is not entirely trivial. The simplest approach is plotting directly the matrix of pairwise distances: temp