Determine Double-Hit Genes
determine_double_hit_genes(
annovar_csv_path,
scna_genes_df,
log2_hom_loss_threshold = -1,
batch_analysis = FALSE
)
path to 'ANNOVAR' csv output file
data frame of gene-level SCNAs (can be output of create_gene_level_scna_df
)
to determine double-hit events, the log2 threshold for identifying homozygous loss events (default = -1).
boolean to indicate whether to perform batch analysis
(TRUE
, default) or personalized analysis (FALSE
). If TRUE
,
a column named 'tumor_id' should be present in both the ANNOVAR csv and the SCNA
table.
vector of gene symbols that are subject to double-hit event(s), i.e. non-synonymous mutation + homozygous copy-number loss