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# loading requried libraries
library(tidyverse)
library(GenomicRanges)
library(TxDb.Mmusculus.UCSC.mm10.knownGene)
library(BSgenome.Mmusculus.UCSC.mm10)
# transcript annotation (bed)
mm10_chr1_trans <- transcripts(TxDb.Mmusculus.UCSC.mm10.knownGene,
filter = list(CDSCHROM = 'chr1'),
columns = c('tx_id', 'gene_id'))
transcripts <- mm10_chr1_trans[!is.na(as.character(mm10_chr1_trans$gene_id))]
sim_transcripts <- promoters(transcripts, downstream = 100000, upstream = 100000)
# simulate stats
set.seed(123)
sim_transcripts$stat1 <- rnorm(length(sim_transcripts), 0, 10)
set.seed(321)
sim_transcripts$stat2 <- rnorm(length(sim_transcripts), 0, 10)
usethis::use_data(sim_transcripts, overwrite = TRUE)
# simulate peaks
set.seed(1234)
n = 10000
distances <- rnorm(n, 0, 5000)
widths <- sample(100:500, n, replace = TRUE)
sim_peaks <- tibble(seqname = 'chr1',
start = sample(start(transcripts), n, replace = TRUE) + abs(distances)/2,
end = start + widths,
peak_name = paste0('peak_', 1:n)) %>%
makeGRangesFromDataFrame(keep.extra.columns = TRUE)
usethis::use_data(sim_peaks, overwrite = TRUE)
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