library(tidyverse)
library(tidyBulk)
# Bhupinder samples
path = "~/third_party_analyses/Bhupinder_oligo_breast"
load(sprintf("%s/results_seurat_together.rda", path))
tt =
dir(
sprintf("%s/bulkRNA/alignment_hg38", path),
pattern = "bam",
recursive = T,
full.names = T
) %>%
grep("Undetermined", ., invert = T, value = T) %>%
tidyBulk_SAM_BAM(genome = "hg38")
tt %>%
filter(transcript %>% is.na %>% `!`) %>%
scale_abundance() %>%
ggplot(aes(count_scaled +1, group=sample)) +
geom_density() +
scale_x_log10()
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