crohn: Crohn's disease data
In snplinkage: Single Nucleotide Polymorphisms Linkage Disequilibrium Visualizations
crohn R Documentation
Crohn's disease data
Description
The data set consist of 103 common (>5% minor allele frequency) SNPs
genotyped in 129 trios from an European-derived population. These
SNPs are in a 500-kb region on human chromosome 5q31 implicated as
containing a genetic risk factor for Crohn disease.
Imported from the gap R package.
An example use of the data is with the following paper,
Kelly M. Burkett, Celia M. T. Greenwood, BradMcNeney, Jinko Graham.
Gene genealogies for genetic association mapping, with application to Crohn's disease.
Fron Genet 2013, 4(260) doi: 10.3389/fgene.2013.00260
Usage
data(crohn)
Format
A data frame containing 387 rows and 212 columns
Source
MJ Daly, JD Rioux, SF Schaffner, TJ Hudson, ES Lander (2001)
High-resolution haplotype structure in the human genome Nature
Genetics 29:229-232
snplinkage documentation built on Sept. 11, 2024, 6:02 p.m.
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| crohn | R Documentation |
Crohn's disease data
Description
The data set consist of 103 common (>5% minor allele frequency) SNPs genotyped in 129 trios from an European-derived population. These SNPs are in a 500-kb region on human chromosome 5q31 implicated as containing a genetic risk factor for Crohn disease.
Imported from the gap R package.
An example use of the data is with the following paper, Kelly M. Burkett, Celia M. T. Greenwood, BradMcNeney, Jinko Graham. Gene genealogies for genetic association mapping, with application to Crohn's disease. Fron Genet 2013, 4(260) doi: 10.3389/fgene.2013.00260
Usage
data(crohn)Format
A data frame containing 387 rows and 212 columns
Source
MJ Daly, JD Rioux, SF Schaffner, TJ Hudson, ES Lander (2001) High-resolution haplotype structure in the human genome Nature Genetics 29:229-232
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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