Description Usage Arguments Value Author(s) References See Also Examples
View source: R/NucleotideDiversity.R
Computes the mean pairwise genetic distance between sequences in the alignment.
1 | NucleotideDiversity(dst,w=NULL)
|
dst |
A "dist" object or a symmetrical matrix with haplotype pairwise distances (ie, the output of DNA.dist). |
w |
An optional numeric vector with the haplotype counts. When |
A value that corresponds to the nucleotide diversity, either by entity or
abundance, depending on argument w
.
Mercedes Guerrero-Murillo and Josep Gregori
Gregori J, Perales C, Rodriguez-Frias F, Esteban JI, Quer J, Domingo E. Viral quasispecies complexity measures. Virology. 2016 Jun;493:227-37. doi: 10.1016/j.virol.2016.03.017. Epub 2016 Apr 6. Review. PubMed PMID: 27060566.
Gregori J, Salicrú M, Domingo E, Sanchez A, Esteban JI, Rodríguez-Frías F, Quer J. Inference with viral quasispecies diversity indices: clonal and NGS approaches. Bioinformatics. 2014 Apr 15;30(8):1104-1111. Epub 2014 Jan 2. PubMed PMID: 24389655.
1 2 3 4 5 6 7 8 9 | # Load haplotype alignment with abundances.
filepath<-system.file("extdata","ToyData_10_50_1000.fna", package="QSutils")
lst <- ReadAmplSeqs(filepath,type="DNA")
# Compute the DNA distance matrix.
dst <- DNA.dist(lst$hseqs,model="K80")
NucleotideDiversity(dst, lst$nr)
NucleotideDiversity(dst)
|
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.