hwe {gap} | R Documentation |
Hardy-Weinberg equlibrium test for a multiallelic marker
Description
Hardy-Weinberg equlibrium test for a multiallelic marker
Usage
hwe(data, data.type = "allele", yates.correct = FALSE, miss.val = 0)
Arguments
data |
A rectangular data containing the genotype, or an array of genotype counts. |
data.type |
An option taking values "allele", "genotype", "count" if data is alleles, genotype or genotype count. |
yates.correct |
A flag indicating if Yates' correction is used for Pearson |
miss.val |
A list of missing values. |
Details
Hardy-Weinberg equilibrium test.
This function obtains Hardy-Weinberg equilibrium test statistics. It can handle data coded as allele numbers (default), genotype identifiers (by setting data.type="genotype") and counts corresponding to individual genotypes (by setting data.type="count") which requires that genotype counts for all n(n+1) possible genotypes, with n being the number of alleles.
For highly polymorphic markers when asymptotic results do not hold, please resort to hwe.hardy
.
Value
The returned value is a list containing:
allele.freq Frequencies of alleles.
x2 Pearson
\chi^2
.p.x2 p value for
\chi^2
.lrt Log-likelihood ratio test statistic.
p.lrt p value for lrt.
df Degree(s) of freedom.
rho
\sqrt{\chi^2/N}
the contingency table coefficient.
Author(s)
Jing Hua Zhao
See Also
Examples
## Not run:
a <- c(3,2,2)
a.out <- hwe(a,data.type="genotype")
a.out
a.out <- hwe(a,data.type="count")
a.out
require(haplo.stats)
data(hla)
hla.DQR <- hwe(hla[,3:4])
summary(hla.DQR)
# multiple markers
s <- vector()
for(i in seq(3,8,2))
{
hwe_i <- hwe(hla[,i:(i+1)])
s <- rbind(s,hwe_i)
}
s
## End(Not run)