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
)

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

extraNotes

vector of strings that are extra source notes to be displayed at the bottom of the 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; if the width is not large enough, text will wrap or table will be cut off

colWidth1

width of "Pangolin Lineage" column; if NULL, widths are automatically assigned to try to fit all text

colWidth2

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