View source: R/ldlinkr_ldproxy_batch.R
| ldlinkr_ldproxy_batch | R Documentation |
Wrapper for LDlinkR::LDproxy_batch.
Easy to use but doesn't scale up well to many SNPs (takes way too long).
ldlinkr_ldproxy_batch(
snp,
pop = "CEU",
r2d = "r2",
min_corr = FALSE,
save_dir = NULL,
verbose = TRUE
)
snp |
a character string or data frame listing rsID's or chromosome coordinates (e.g. "chr7:24966446"), one per line |
pop |
a 1000 Genomes Project population, (e.g. YRI or CEU), multiple allowed, default = "CEU" |
r2d |
either "r2" for LD R2 or "d" for LD D', default = "r2" |
min_corr |
Minimum correlation with |
save_dir |
Save folder. |
verbose |
Print messages. |
merged_query_dat <- echodata::get_Nalls2019_merged()
lead.snps <- setNames(subset(merged_query_dat, leadSNP)$Locus,
subset(merged_query_dat, leadSNP)$SNP)
proxies <- ldlinkr_ldproxy_batch(snp = lead.snps)
Other LD:
check_population_1kg(),
compute_LD(),
filter_LD(),
get_LD(),
get_LD_1KG(),
get_LD_1KG_download_vcf(),
get_LD_UKB(),
get_LD_matrix(),
get_LD_vcf(),
get_locus_vcf_folder(),
plot_LD(),
popDat_1KGphase1,
popDat_1KGphase3,
rds_to_npz(),
saveSparse(),
save_LD_matrix(),
snpstats_get_MAF()
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