-
UNNECESSARY: consider how to keep sashimi plot updates to one pass, preventing sample_id and gene changes from being out of sync, and triggering a partial update to the plot before both are ready.
get_sashimi_data()
might be that step
-
UNNECESSARY: move memoise function definitions outside the reactive({}) blocks
- e.g. prepareSashimi_m
- also check
use_memoise
and create non-memoise version
-
UNNECESSARY: move gene_exon_structure
gene2gg()
into separate reactive function that depends upon:
show_gene_model_d() # if FALSE then return NULL
flatExonsByGene1 <- get_flat_gene_exons_plot();
gene <- get_active_gene();
get_gene_coords()
exonLabelSize=14 + exon_label_size_d() + font_sizing_d()
- consider moving plotly sashimi creation into separate function
gg_ly <- get_plotly_sashimi() # reactive
- consider moving ggplot2 sashimi creation into separate function
gg_ly <- getgg_plot2_sashimi() # reactive
-
COMPLETE: allow gene/transcript/exon model panel height to be adjusted
-
TODO: when there are 2+ panel columns, display gene model below each column
-
TODO: when "show detected transcripts" is not checked, re-calculate flat exons for that gene
-
organize dependency tree and see if there are shortcuts in the process
-
File issue with ggrepel, ask if labels outside plot range can be hidden, for example when using
coord_cartesian()
to limit visual range.