magnify_to_sampled_freq: Multiplies sequence data up to sampled frequency, aligns and...

Description Usage Arguments Details

View source: R/magnify_to_sampled_freq.R

Description

magnify_to_sampled_freq

Usage

1
magnify_to_sampled_freq(directory_path = getwd(), magnify_file_list)

Arguments

directory_path

path to the directory in which to build/call files, defaults to working directory

magnify_file_list

.csv file with two columns; first column lists accession numbers/accession versions and the second the frequency that haplotype was found at when sampled.

Details

Function multiplies data to sampled frequency, aligns sequences, writes aligned fasta files, plots haplotype network and extracts summary data.

Unaligned sequence files are read in and accessions (individual haplotypes) are multiplied by given values in relevant .csv file. Also, haplotype networks are drawn, and summary data recorded.


EvolEcolGroup/mtDNAcombine documentation built on July 8, 2021, 10:30 p.m.