| get.vcf | R Documentation |
Generate a vcf-file for selected groups and chromosome
get.vcf(
population,
path = NULL,
database = NULL,
gen = NULL,
cohorts = NULL,
id = NULL,
chromosome = "all",
non.genotyped.as.missing = FALSE,
use.id = FALSE,
file.append = FALSE
)
population |
Population list |
path |
Location to save vcf-file |
database |
Groups of individuals to consider for the export |
gen |
Quick-insert for database (vector of all generations to export) |
cohorts |
Quick-insert for database (vector of names of cohorts to export) |
id |
Individual IDs to search/collect in the database |
chromosome |
Limit the genotype output to a selected chromosome (default: "all") |
non.genotyped.as.missing |
Set to TRUE to replaced non-genotyped entries with "./." |
use.id |
Set to TRUE to use MoBPS ids instead of Sex_Nr_Gen based names |
file.append |
Set extend an existing vcf-file ((without writting a header)) |
VCF-file for in gen/database/cohorts selected individuals
data(ex_pop)
file_path <- tempdir()
get.vcf(path=file_path, ex_pop, gen=2)
file.remove(paste0(file_path, ".vcf"))
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