makeAssaySummaryTables.Rd
Make 2 tables, a version with all mutations from the subset database, and a version with high-risk mutations; displays mutated sequence counts categorized by assay and number of assays affected on top and by variant on the left
makeAssaySummaryTables(
DB,
variantFile,
extraNotes = NULL,
saveTable = FALSE,
saveFolder = NULL,
height = NULL,
width = NULL,
colWidth1 = NULL,
colWidth2 = NULL
)
File path to subset database file. In the case of making summary tables, we use the
3M version from CoMIT, returned from pull_subset_DB()
csv file containing "Displayed_Lineage_Order" column for ordering row names/row groups in the GT table
vector of strings that are extra source notes to be displayed at the bottom of the table
logical value indicating whether to save the tables to the specified saveFolder
file path containing folder the finished tables will be saved in
desired height of table .png images
desired width of table .png images; if the width is not large enough, text will wrap or table will be cut off
width of "Pangolin Lineage" column; if NULL, widths are automatically assigned to try to fit all text
width of all other columns; if NULL, widths are automatically assigned to try to fit all text