
Function that gathers data tables on diagnostic variants
Source:R/biomarkers.R
prep_diagn_display_tbl.RdFunction that gathers data tables on diagnostic variants
Arguments
- rep
report object
- tier
tier level(s) to consider for display (e.g. 1, 2)
- etype_for_tiering
evidence type(s) to consider for tiering (e.g. 'diagnostic')
- clnsig
clinical significance to consider for tiering (e.g. 'diagnostic_positive', 'diagnostic_negative')
- tier_defining_eitems_only
consider only evidence items that were used for tiering (e.g. for tier 1: only evidence items with A-level evidence, for tier 2: only evidence items with B-level evidence). If FALSE, all evidence items associated with each variant, not only the tier-defining evidence items, will be considered for display in the report.
- variant_category
cna, snv_indel, or fusion