cystic_fibrosis_snps_df | R Documentation |
This dataset, cystic_fibrosis_snps_df, is a data frame containing genetic association data for cystic fibrosis, including a case-control indicator and 23 single nucleotide polymorphisms (SNPs) with specified inter-marker distances. The dataset contains 186 observations across 24 variables.
data(cystic_fibrosis_snps_df)
A data frame with 186 observations and 24 variables:
Integer case-control indicator
Integer SNP genotype at location 1
Integer SNP genotype at location 2
Integer SNP genotype at location 3
Integer SNP genotype at location 4
Integer SNP genotype at location 5
Integer SNP genotype at location 6
Integer SNP genotype at location 7
Integer SNP genotype at location 8
Integer SNP genotype at location 9
Integer SNP genotype at location 10
Integer SNP genotype at location 11
Integer SNP genotype at location 12
Integer SNP genotype at location 13
Integer SNP genotype at location 14
Integer SNP genotype at location 15
Integer SNP genotype at location 16
Integer SNP genotype at location 17
Integer SNP genotype at location 18
Integer SNP genotype at location 19
Integer SNP genotype at location 20
Integer SNP genotype at location 21
Integer SNP genotype at location 22
Integer SNP genotype at location 23
The dataset name has been kept as 'cystic_fibrosis_snps_df' to avoid confusion with other datasets in the R ecosystem. This naming convention helps distinguish this dataset as part of the DigestiveDataSets package and assists users in identifying its specific characteristics. The suffix 'df' indicates that the dataset is a data frame. The original content has not been modified in any way.
Data taken from the gap.datasets package version 0.0.6. Original source: Liu JS, Sabatti C, Teng J, Keats BJB, Risch N (2001). "Bayesian Analysis of Haplotypes for Linkage Disequilibrium Mapping". Genome Research, 11:1716–1724.
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