Description Usage Arguments Value Author(s) References See Also Examples
Computes the table of mutation frequencies by position with respect to the alignment consensus.
1 |
hseqs |
DNAStringSet or AAStringSet with the aligned haplotype sequences. |
nr |
An optional numeric vector with the haplotype counts. When |
Matrix of mutation counts by position. A (4 x n) or (20 x n) matrix, where n is the alignment length.
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 the haplotypes alignment with abundances.
filepath<-system.file("extdata","ToyData_10_50_1000.fna", package="QSutils")
lst <- ReadAmplSeqs(filepath,type="DNA")
# Table of mutations in the alignment, regardless of haplotype abundance.
MutsTbl(lst$hseqs)
# Table of mutations taking into account abundance.
MutsTbl(lst$hseqs,lst$nr)
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