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TREE

Topological REcombination Estimator

Authors: Devon P. Humphreys, Melissa R. McGuirl, Michael Miyagi, Andrew J. Blumberg

For questions/comments please contact Melissa R. McGuirl at [email protected].

Description

This software takes as input either (1) a collection of genomes in FASTA format or (2) a distance matrix and predicts the underlying recombination rate from topological summary statistics of the data. The supported distance matrix formats are those formats that are currently supported by Ripser:

  • comma-separated values lower triangular distance matrix (preferred)
  • comma-separated values upper triangular distance matrix (MATLAB output from the function pdist)
  • comma-separated values full distance matrix

The user has the option getting recombination rate estimates over a sliding window analysis and can specify a normalization factor (default = 1/1000).

This software is based upon the work presented in Humphreys, D.P., McGuirl, M.R., Miyagi, M., and Blumberg, A.J. Fast Estimation of Recombination Rates Using Topological Data Analysis (2018). Preprint: https://www.biorxiv.org/content/early/2018/08/20/395210

Getting Started

These instructions will get you a copy of the project up and running on your local machine for development and testing purposes. See deployment for notes on how to deploy the project on a live system.

Prerequisites

Programs

Python libraries

  • ripser
  • matplotlib
  • numpy

Install the ripser program as follows:

	pip install Cython
	pip install Ripser

TREE Source

      cd 
      git clone https://github.com/MelissaMcguirl/TREE
      cd TREE
      pip install -r requirements.txt

Usage:

      python TREE.py -i INPUT_FILE [-t INPUT_TYPE] [-s SLIDING_WINDOW_FLAG] [-w WINDOW_SIZE] [-o OUTPUT_DIRECTORY] [-N NORMALIZATION_FACTOR] [-n FILENAME_IDENTIFIER] [-b BASE_FLAG] [-f OFFSET_VALUE] [-g PLOT_NAME]

Note, the default input type is a FASTA file and the default normalization factor is 1/1000.

Examples:

      cd src
      1) python TREE.py -i ../examples/seq_example.fasta (input = FASTA file)   
      2) python TREE.py -i ../examples/hamming_example -t DIST (input = distance matrix)
      3) python TREE.py -i ../examples/seq_example.fasta -s -w 20 -o ../examples/outputs -n test -g ../examples/outputs/outputPlt (sliding window analysis over SNPs)
      4) python TREE.py -i ../examples/seq_example.fasta -s -b -w 20 -f 10 -o ../examples/outputs -n test -g ../examples/outputs/outputPlt (sliding window analysis over raw bases)

Outputs:

  Sample expected output plot and text file of predictions for the sliding window analysis is provided in examples/outputs/

Pipeline:

  0) Compute Hamming distance matrix
  1) Feed Hamming distance matrix into Ripser to compute dimension 0 and dimension 1 persistent homology barcodes
  2) Extract topological summary statistics (psi, b1, phi)
  3) Predict recombination rate using TREE
  4) Plot results and save predictions to text file (for sliding windows)

Help:

  python TREE.py -h

Notes

This software has been tested with python 2.7 and 3.6.1.

tree's People

Contributors

devonhum avatar edguy3 avatar

Stargazers

Hugo de Paula Oliveira avatar Sofía Goy avatar  avatar Rimjhim Roy Choudhury avatar  avatar Scott T Small avatar  avatar

Watchers

James Cloos avatar  avatar  avatar  avatar Mia Miyagi avatar Melissa McGuirl avatar

Forkers

edguy3 unlhcc

tree's Issues

NA bug

Hi:
When estimating the rho of multiple populations simultaneously, if the genotype of a population in a particular window is all NA, then the output of this population will be one less window than other populations.

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