Make 2 tables (one version with all mutated sequences and one version with sequences with high-risk mutations) showing mutated sequence counts categorized by number of assays affected on top and by variant on the left

makeCoOccTables(
  DB,
  variantFile,
  saveTable = FALSE,
  saveFolder = NULL,
  height = NULL,
  width = NULL,
  colWidth1 = NULL,
  colWidth2 = NULL
)

Arguments

DB

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()

variantFile

csv file containing "Displayed_Lineage_Order" column for ordering row names/row groups in the GT table

saveTable

logical value indicating whether to save the tables to the specified saveFolder

saveFolder

file path containing folder the finished tables will be saved in

height

desired height of table .png images

width

desired width of table .png images

colWidth1

width of "Pangolin Lineage" and "WHO Label" columns in px; if NULL, widths are automatically assigned to try to fit all text

colWidth2

width of all other columns in px; if NULL, widths are automatically assigned to try to fit all text