Last data update: 2014.03.03

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CranContrib
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Results 1 - 4 of 4 found.
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Alzheimer (Package: HardyWeinberg) : Genotype frequencies for 70 SNPs related to Alzheimer's disease

The dataframe contains the genotype frequencies MM, Mm and mm for the 70 SNPs for both cases and controls. The data are taken from table 7.11 in Laird & Lange.
● Data Source: CranContrib
● Keywords: datasets
● Alias: Alzheimer
● 0 images

HapMapCHBChr1 (Package: HardyWeinberg) : Genotype frequencies for 225 SNPs on chromosome 1 of the CHB population.

The dataframe contains the genotype frequencies in generic notation, AA, AB and BB the first 225 polymorphic SNPs without missing data on chromosome 1 of the Han Chinese in Beijing. The data are compiled from the HapMap project, phase 3.2, containing genotype information of 84 individuals.
● Data Source: CranContrib
● Keywords: datasets
● Alias: HapMapCHBChr1
● 0 images

Mourant (Package: HardyWeinberg) : Genotype frequencies for blood group locus MN

The dataframe contains the genotype frequencies MM, MN and NN for the MN blood group locus for 216 populations. The data are taken from table 2.5 in Mourant et al., using only entries with a sample size of at least 500.
● Data Source: CranContrib
● Keywords: datasets
● Alias: Mourant
● 0 images

Markers (Package: HardyWeinberg) : SNP data and intensities

The dataframe contains the genotypes of 3 SNPs and two allele intensities of 146 individuals. The first column is a GT polymorphism that has missing values for several individuals. The second and third column (iG and iG) are the allele intensities of this polymorphism. Column 4 and 5 are covariate SNPs (an AC and an AG polymorphism) that have no missing values.
● Data Source: CranContrib
● Keywords: datasets
● Alias: Markers
● 0 images