LDpair | R Documentation |
Investigates potentially correlated alleles for a pair of variants.
LDpair(
var1,
var2,
pop = "CEU",
token = NULL,
output = "table",
file = FALSE,
genome_build = "grch37",
api_root = "https://ldlink.nih.gov/LDlinkRest"
)
var1 |
the first RS number or genomic coordinate (e.g. "chr7:24966446") |
var2 |
the second RS number or genomic coordinate (e.g. "ch7:24966446") |
pop |
a 1000 Genomes Project population(s), (e.g. YRI or CEU), multiple allowed, default = "CEU" |
token |
LDlink provided user token, default = NULL, register for token at https://ldlink.nih.gov/?tab=apiaccess |
output |
two output options available, "text", which displays a two-by-two matrix displaying haplotype counts and allele frequencies along with other statistics, or "table", which displays the same data in rows and columns, default = "table" |
file |
Optional character string naming a path and file for saving results. If file = FALSE, no file will be generated, default = FALSE. |
genome_build |
Choose between one of the three options...'grch37' for genome build GRCh37 (hg19), 'grch38' for GRCh38 (hg38), or 'grch38_high_coverage' for GRCh38 High Coverage (hg38) 1000 Genome Project data sets. Default is GRCh37 (hg19). |
api_root |
Optional alternative root url for API. |
text or data frame, depending on the output option
## Not run: LDpair(var1 = "rs3", var2 = "rs4", pop = "YRI", token = Sys.getenv("LDLINK_TOKEN"))
## Not run: LDpair("rs3", "rs4", "YRI", token = Sys.getenv("LDLINK_TOKEN"), "text")
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