| Title: | Data used in the examples and vignettes of the GWASTools package |
|---|---|
| Description: | Selected Affymetrix and Illlumina SNP data for HapMap subjects. Data provided by the Center for Inherited Disease Research at Johns Hopkins University and the Broad Institute of MIT and Harvard University. |
| Authors: | Stephanie Gogarten |
| Maintainer: | Stephanie Gogarten <[email protected]> |
| License: | Artistic-2.0 |
| Version: | 1.50.0 |
| Built: | 2026-10-10 11:03:02 UTC |
| Source: | https://github.com/bioc/GWASdata |
Selected Affymetrix and Illlumina SNP data for HapMap subjects. Data provided by the Center for Inherited Disease Research (CIDR) at Johns Hopkins University and the Broad Institute of MIT and Harvard University.
77 HapMap subjects were genotyped by CIDR on the Illumina Human1Mv_C array. Selected data includes 1000 SNPs on each of chromosomes 21, 22, and X, and 100 SNPs on each of Y, the pseudoautosomal region, and mitochondrial DNA. SNP and scan annotation are provided as R data frames. Genotype data, X and Y intensity data with quality scores, and B allele frequency / log R ratio data are stored in NetCDF files. Text files with raw data are provided for 3 subjects.
47 of the HapMap subjects were genotyped by the Broad on the Affymetrix GenomeWideSNP_6 array. Identical SNPs to the Illumina data were selected for chromosomes 21, 22, and X. SNP and scan annotation are provided as R data frames. Genotype data and X and Y intensity data with quality scores are stored in NetCDF files. Text files with raw data are provided for 3 subjects.
List of datasets:
affy_scan_annot: data.frame with Affymetrix scan annotation
affy_snp_annot: data.frame with Affymetrix SNP annotation
affyScanADF: ScanAnnotationDataFrame with Affymetrix scan annotation
affySNPADF: SnpAnnotationDataFrame with Affymetrix
SNP annotation
illumina_scan_annot: data.frame with Illumina scan annotation
illumina_snp_annot: data.frame with Illumina SNP annotation
illuminaScanADF: ScanAnnotationDataFrame with Illumina scan annotation
illuminaSnpADF: SnpAnnotationDataFrame with Illumina
SNP annotation
List of files in "extdata":
affy_geno.nc: NetCDF file with Affymetrix genotypes
affy_qxy.nc: NetCDF file with Affymetrix XY intensity data and quality scores
affy_raw_data: Directory with Affymetrix raw data in text files
illumina_geno.nc: NetCDF file with Illumina genotypes
illumina_qxy.nc: NetCDF file with Illumina XY intensity data and quality scores
illumina_bl.nc: NetCDF file with Illumina BAlleleFreq and LogRRatio data
illumina_geno.gds: GDS file with Illumina genotypes
illumina_qxy.gds: GDS file with Illumina XY intensity data and quality scores
illumina_bl.gds: GDS file with Illumina BAlleleFreq and LogRRatio data
illumina_raw_data: Directory with Illumina raw data in text files
illumina_subj.ped: PLINK PED file with Illumina genotypes
illumina_subj.map: PLINK MAP file with Illumina SNP info
illumina_subj.bim: PLINK extended MAP file with Illumina SNP info and alleles
ScanAnnotationDataFrame,
SnpAnnotationDataFrame,
NcdfGenotypeReader, NcdfIntensityReader,
GdsGenotypeReader, GdsIntensityReader,
GenotypeData, IntensityData
library(GWASdata) data(illumina_scan_annot) data(illumina_snp_annot) data(illuminaScanADF) # ScanAnnotationDataFrame data(illuminaSnpADF) # SnpAnnotationDataFrame varMetadata(illuminaSnpADF) # NetCDF file <- system.file("extdata", "illumina_geno.nc", package="GWASdata") nc <- NcdfGenotypeReader(file) geno <- getGenotype(nc, snp=c(1,10), scan=c(1,5)) genoData <- GenotypeData(nc, snpAnnot=illuminaSnpADF, scanAnnot=illuminaScanADF) # GDS file <- system.file("extdata", "illumina_geno.gds", package="GWASdata") gds <- GdsGenotypeReader(file) geno <- getGenotype(gds, snp=c(1,10), scan=c(1,5)) genoData <- GenotypeData(gds, snpAnnot=illuminaSnpADF, scanAnnot=illuminaScanADF) # raw data list.files(system.file("extdata", "illumina_raw_data", package="GWASdata"))library(GWASdata) data(illumina_scan_annot) data(illumina_snp_annot) data(illuminaScanADF) # ScanAnnotationDataFrame data(illuminaSnpADF) # SnpAnnotationDataFrame varMetadata(illuminaSnpADF) # NetCDF file <- system.file("extdata", "illumina_geno.nc", package="GWASdata") nc <- NcdfGenotypeReader(file) geno <- getGenotype(nc, snp=c(1,10), scan=c(1,5)) genoData <- GenotypeData(nc, snpAnnot=illuminaSnpADF, scanAnnot=illuminaScanADF) # GDS file <- system.file("extdata", "illumina_geno.gds", package="GWASdata") gds <- GdsGenotypeReader(file) geno <- getGenotype(gds, snp=c(1,10), scan=c(1,5)) genoData <- GenotypeData(gds, snpAnnot=illuminaSnpADF, scanAnnot=illuminaScanADF) # raw data list.files(system.file("extdata", "illumina_raw_data", package="GWASdata"))