Description Usage Arguments Details
View source: R/magnify_to_sampled_freq.R
magnify_to_sampled_freq
1 | magnify_to_sampled_freq(directory_path = getwd(), magnify_file_list)
|
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. |
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.
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