View source: R/imputationPipeline.R
| createGenomewideDosage | R Documentation |
Inputs are VCF files, one for each chromosome presumably.
createGenomewideDosage(pathIn, chroms, nameOfchromWiseDosageFiles)
nameOfchromWiseDosageFiles |
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:
Output is an .rds (R dataset) format.
Other imputation_functions:
convertDart2vcf(),
convertVCFtoDosage(),
filter_positions(),
mergeVCFs(),
postImputeFilterBeagle4pt1(),
postImputeFilter(),
runBeagle4pt1GL(),
runBeagle5(),
splitVCFbyChr()
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