#' @importFrom rlang .data
#' @importFrom dplyr select
#'
snpinfo_to_haplos <- function(snpinfo) {
# This routine is brittle. It depends on specific names in snpinfo and/or nc.
alleles <- names(dplyr::select(
snpinfo,
-(.data$snp_id:.data$alleles)))
# Would be better to have object that gives allele names rather than this opposite approach.
infonames <- c("consequence","type","sdp","index","interval","on_map","pheno","lod","ensembl_gene")
m <- match(alleles, infonames)
alleles <- alleles[is.na(m)]
# Columns in between consequence and type should be alleles.
# If not provided, assume we are in mouse with 8.
if((nc <- length(alleles)) < 2) {
warning("no alleles in snpinfo; assuming 8")
nc <- 8
}
LETTERS[seq_len(nc)]
}
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