View source: R/semicontinuousMixtureInterpretation.R
This takes the output of: getMitoGenomes and indexes it. In particular, it extracts the unique haplotypes, adds the haplotype ID to the genomes themselves, and it returns a list of exactly 2 items. The first is a dataframe with the genomes data frame with an n column added (# of times the haplotype was seen) as well as a SeqID (unique ID) the second is a dataframe with the haplotype sequence, n (# of times seen in database, total), and the same SeqID
1 | preprocessMitoGenomes(genomes)
|
genomes |
a data frame from MMDIT::getMitoGenomes |
Add the following code to your website.
For more information on customizing the embed code, read Embedding Snippets.