# create function to find the exons of any gene in homosapien
#' Title
#'
#' @param gene is a string for the gene using RefSeq IDs
#'
#' @return a dataframe of the exons, and their positions within the genome
#'
#' @export
#'
#' @examples
#'
#' find_exons("NM_000059")
#'
find_exons <- function(gene) {
# create ensembl using grch37.ensembl for homosapien
ensembl <-
biomaRt::useMart(
biomart = "ENSEMBL_MART_ENSEMBL",
host = "grch37.ensembl.org",
path = "/biomart/martservice",
dataset = "hsapiens_gene_ensembl"
)
# retrieve the exons and their positions within the genome
exons <- biomaRt::getBM(
attributes = c(
'chromosome_name',
'exon_chrom_start',
'exon_chrom_end',
'5_utr_start',
'5_utr_end',
'3_utr_start',
'3_utr_end'
),
filters = "refseq_mrna",
values = gene,
bmHeader = TRUE,
mart = ensembl
)
exons <- exons %>%
dplyr::rename_all(
.funs = function(.x) {
.x %>% tolower() %>% stringr::str_replace_all(pattern = " |\\)|\\(", replacement = "_")
}
) %>%
dplyr::mutate(exon_length = exon_region_end__bp_ - exon_region_start__bp_)
return(exons)
}
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