Homework 3: Phylogeny Inference Solution

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Instructions Please turn this assignment in on the course web page. There are multiple files to turn in. All text and code should be placed into a single folder with a name like ​lastname_exerciseXX​. The folder should then be compressed and submitted as a single archive (.zip or .tgz) You must do this work on…

5/5 – (2 votes)

You’ll get a: zip file solution

 

Description

5/5 – (2 votes)

Instructions

  • Please turn this assignment in on the course web page.

  • There are multiple files to turn in. All text and code should be placed into a single folder with a name like lastname_exerciseXX. The folder should then be compressed and submitted as a single archive (.zip or .tgz)

  • You must do this work on your own, although you are encouraged to have general discussions with other students. The work you turn in must be your own. Your code will be checked for overlap and for surprising idiosyncrasies in common with other submissions.

  • Please write the names of all students with whom you discussed the assignment at the top of your code.

  • Please include copious comments in your code. Full credit will only be given for code that is fully commented, meaning that every line that is not completely obvious needs a comment. Partial credit may be given for broken/non-functioning code if the code is well-commented.

  • You may use any programming language you wish.

Background

This homework assignment is an implementation of the Nei-Saitou neighbor-joining algorithm for phylogeny construction, with estimation of bootstrap support.

Datasets

Download and extract the data: https://www.dropbox.com/s/81cqr72rpfgwnhy/Homework3.zip?dl=1.

If you will be using the supplied scripts for visualizing your tree (hw3-plot-newick.ror hw3-plot-edges.r), then you will need to install R(Google it), then install the “ape” package and the “RColorBrewer” package by running R, and then entering this command:

install.packages(c(‘ape’,’RColorBrewer’))

hw3.fna

File containing a multiple alignment of 61 bacterial 16S subunit ribosomal RNA sequences.

hw-tip-labels.txt

File containing tab-delimited rows of this format:

seqID Phylum color

There is a subfolder called solution. This contains examples of correct output:

solution/hw3-solution-genetic-distances.txt

Genetic distances (% different) between every pair of sequences in hw3.fna.

solution/hw3-nj-solution-edges.txt

Correct edges for neighbor-joining tree using R implementation, in preorder traversal order. Your edge order and internal node labels do not need to be exactly the same.

solution/hw3-nj-solution-bootstrap.txt

Example bootstrap support values for the 59 internal nodes in preorder traversal order.

solution/tree.pdf, solution/tree-bootstrap.pdf

Example PDF plot of tree showing colored tips and bootstrap support (bonus) for internal nodes.

solution/hw3-nj-solution-tree.tre

Correct solution output tree in NEWICK format. Your node order does not need to be exactly the same.

Input and Output Format:

Your program should take one command line argument specifying the name of a sequence file. The command line should be of the form programName sequence.fastaor programName -i sequence.fasta(it is acceptable to invoke java or another program as part of programName, but only take one argument as input).

Your program should output two files:

edges.txt

This file is tab delimited. Each row describes an edge in the tree. The first column is the ancestor node; the second column is the descendant node; the third column is the edge length. Edges should be in preorder traversal order choosing any internal node as the root. Tips must be indexed starting at 1, with 1 corresponding to the first sequence in the FASTA file, 2 corresponding to the second sequence, and so on. The internal nodes should begin numbering at the root with ntips + 1and the numbers should increase according to preorder traversal.

tree.txt

This file is in NEWICK format with all edge distances and with only tips named. For example, The following tree would be encoded (A:0.1,B:0.2,(C:0.3,D:0.4):0.5) :

Problems

  1. (25 points): Read in the given FASTA file hw3.fna. Calculate the genetic distance (% dissimilarity) between every pair of sequences, and write this to a tab-delimited file with rows and columns labeled by the sequence identifiers. For pairwise dissimilarity calculations, you may count a gap in both sequences as a similarity.

  1. (25 points): Implement Nei-Saitou neighbor joining as described on Wikipedia

(https://en.wikipedia.org/wiki/Neighbor_joining) and/or in class notes. Provide extensive comments in your code. I suggest that you store your tree in this data structure, but you can do it however you want:

edges, A 3-column matrix with column 1 representing an ancestor node, column 2 representing the descendant node, and the final column representing the edge length. Tips should be indexed starting at 1. Choose an arbitrary internal node to be the root. The internal nodes should begin numbering with the root as ntips + 1. An example is shown in solution/hw3-nj-solution-edges.txt.

  1. (25 points): Generate the two output files described above for your tree (edges matrix and NEWICK tree file). For the edges matrix you will need to perform a preorder traversal. For the NEWICK file you will need to perform a postorder traversal. These should be generated using recursive functions.

  1. (25 points): Find a way to visualize your trees from step (3). There are many NEWICK-based viewers online. Colors for the tips are provided in hw-tip-labels.txt. Colors are nice but optional. You must include labels for your tips. ASCII art is acceptable but not preferred. If you made the output correctly for step (3), you can use either of the included R scripts (after installing the “ape” and the “RColorBrewer” package as described above):

Rscript hw3-plot-newick.r hw3-nj-solution-tree.txt hw3-tip-labels.txt or

Rscript hw3-plot-edges.r hw3-nj-solution-edges.txt hw3-tip-labels.txt

Here is what my Nei-Saitou tree looks like:

BONUS (10 points): Perform 100 inferences of the tree in step (3) using bootstrap samples. Each bootstrap sample of the DNA sequences should contain a random rearrangement of the original DNA columns selected by repeated sampling with replacement until there are as many columns as in the original input. This means that some columns will appear more than once in a bootstrap sample. Here is a nice depiction of the resampling that Pin-Kuang showed us in class:

For each node in the original tree, get a list of the tips that are partitioned below it. Count the fraction of bootstrap trees in which the exact same partition was made. That is the bootstrap confidence for the given internal node. You may simply print the bootstrap values to a text file in the order of the indices of your internal nodes as shown in your edges file from step (3). You can also plot the bootstrap confidence using the supplied R scripts (red is fraction with bootstrap support):

Rscript hw3-plot-edges.r hw3-nj-solution-edges.txt hw3-tip-labels.txt boots.txt

Deliverables

Source files (your code for Step 1, 2, 3)

Readme file explaining how to use your code (text)

Step 1 distances file

Step 3 outputs (edges.txt, tree.txt)

Visualization of Step 3 tree

Code for and visualization of Bonus (optional)

All files and source code should be added to a folder with your x500 username as the name of the folder.

Then, zip this folder and upload it on Moodle.

Homework 3: Phylogeny Inference Solution
$30.00 $24.00