Description Usage Arguments Examples
Calculates genetic distance between samples and population references.
1 2 | calculateAMidsArith(pathTotpeds, pathToAriMedoids, AMmcapply = F, nrcores,
seqchip = "", noseqdat = F, wd, NameOut = NULL, pathAll00)
|
pathTotpeds |
Character vector giving path to folder containing the plink tPED file(s) to be used. |
pathToAriMedoids |
Character vector giving path to folder containing the arithmetic references to be used. |
AMmcapply |
Logical value (TRUE or FALSE), specifying if the multicore funcion mcapply, should be used. Inappropriate for most HPC cluster systems. Default = FALSE |
nrcores |
Numeric value detailing how many cores should be used if AMmcapply==TRUE. If left unspecificed the number of cores will be detected and nrcores will be set to that number -2. |
seqchip |
Character vector specifying if only references from one main SNP chip panel are to be used. All references are marked with what chip panel they use at the end of their file names, eg 'Yoruba.HGDP.20000.Illumina.ods' May be important if your data has few SNPs in common with one panel. All toy references prepared use 'Illumina' panels. Whole Genome sequence data is specified with 'WG'. Supports custom designations, but will trigger a warning when used. |
noseqdat |
Logical value (TRUE or FALSE), specifying if sequence data is to be excluded, will use only references that do not have names ending in '.WG.ods/rds/rda'. Default = FALSE |
wd |
Character vector giving the desired working directory to house the outputs of calculateAMidsArith. If left unspecified will use current working directory. |
NameOut |
Character vector giving the desired prefix name for the AMid file. Default is NULL. |
pathAll00 |
Character vector giving the path to a file containing the full data table of each dbSNP and both alleles. An example version covering the SNPs used in the example data is included. A full version can be found at: http://bit.ly/1OUstDP |
1 2 3 4 5 6 7 8 9 10 11 12 13 14 | ## Not run:
Refs <- system.file('data', package = 'AncestryMapper')
tpeds <- system.file('extdata', package = 'AncestryMapper')
Corpheno <- system.file('extdata', 'CorPheno', package = 'AncestryMapper')
All00Frq <- system.file ('data', 'MinMaxFreq.rda', package = 'AncestryMapper')
genetic.distance <- calculateAMidsArith(pathTotpeds = tpeds,
NameOut = 'Example',
pathToAriMedoids = Refs,
pathAll00 = All00Frq)
plotAMids(AMids = genetic.distance, phenoFile = Corpheno, columnPlot = "I")
## End(Not run)
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[1] "Abkhaz.Yunusbayev2011 Finished"
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[1] "tPED files used:"
[1] "/usr/lib/R/site-library/AncestryMapper/extdata/Demo.tped"
[1] "1000 common SNPs found between all submitted tPED files."
[1] "1000 common SNPs found between All00 reference and all submitted tPED files"
[1] "/usr/lib/R/site-library/AncestryMapper/extdata/Demo.tped"
[1] "***** Number of SNPs Used: 1000"
[1] "Wrote out AMid file to, /work/tmp/AMidExample_ref143_inds567_SNPs1000.amid"
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