R/imputationPipeline.R
createGenomewideDosage.Rd
Inputs are VCF files, one for each chromosome presumably.
createGenomewideDosage(pathIn, chroms, nameOfchromWiseDosageFiles)
Output is an .rds (R dataset) format.
Use common naming for VCF with prefix e.g. "chr12_".
Combines "<chroms>_<nameOfchromWiseDosageFiles>".
Output is an .rds (R dataset) format.
NOTICE: This function is part of a family of functions ("imputation_functions"
) developed as part of the NextGen Cassava Breeding Project genomic selection pipeline.
For some examples of their useage:
Other imputation_functions:
convertDart2vcf()
,
convertVCFtoDosage()
,
filter_positions()
,
mergeVCFs()
,
postImputeFilterBeagle4pt1()
,
postImputeFilter()
,
runBeagle4pt1GL()
,
runBeagle5()
,
splitVCFbyChr()