cnrakt/haplotypes: Manipulating DNA Sequences and Estimating Unambiguous Haplotype Network with Statistical Parsimony
Provides S4 classes and methods for reading and manipulating aligned DNA sequences, supporting an indel coding methods (only simple indel coding method is available in the current version), showing base substitutions and indels, calculating absolute pairwise distances between DNA sequences, and collapses identical DNA sequences into haplotypes or inferring haplotypes using user provided absolute pairwise character difference matrix. This package also includes S4 classes and methods for estimating genealogical relationships among haplotypes using statistical parsimony and plotting parsimony networks.
Getting started
Browse package contents
Package details |
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| Author | Caner Aktas |
| Maintainer | Caner Aktas <caktas.aca@gmail.com> |
| License | GPL-2 |
| Version | 1.1.3.1 |
| URL | https://cran.r-project.org https://biolsystematics.wordpress.com/r/ |
| Package repository | View on GitHub |
| Installation |
Install the latest version of this package by entering the following in R:
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