table2hap | R Documentation |
convert variants stored in table format into hapResult
table2hap(x, hapPrefix = "H", pad = 3, hetero_remove = TRUE, na_drop = TRUE)
x |
a data.frame contains variants information. The first file column are fix as Chrome name, position, reference nuclieotide, alter nuclieotide and INFO. Accession genotype should be in followed columns. "-" will be treated as Indel. "." and "N" will be treated as missing data. Heterozygotes should be "A/T", "AAA/A" |
hapPrefix |
prefix of haplotype names |
pad |
The number length in haplotype names should be extend to. |
hetero_remove |
whether remove accessions contains hyb-sites, Character not A T C G |
na_drop |
whether drop accessions contains missing data ("N", "NA", ".") |
object of hapSummary class
data("geneHapR_test")
hapResult <- table2hap(gt.geno, hapPrefix = "H",
hetero_remove = TRUE,
na_drop = TRUE)
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