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# SnpAnnotationDataFrame
# Snp Annotation stored as an AnnotatedDataFrame
setClass("SnpAnnotationDataFrame",
contains = "AnnotatedDataFrame",
representation(idCol = "character",
chromosomeCol = "character",
positionCol = "character",
alleleACol = "character",
alleleBCol = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(idCol = "snpID",
chromosomeCol = "chromosome",
positionCol = "position",
alleleACol = "alleleA",
alleleBCol = "alleleB",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# SnpAnnotationSQLite
# Snp Annotation stored in a SQLite database
setClass("SnpAnnotationSQLite",
representation(dbpath = "character",
dbcon = "SQLiteConnection",
annotationTable = "character",
metadataTable = "character",
idCol = "character",
chromosomeCol = "character",
positionCol = "character",
alleleACol = "character",
alleleBCol = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(idCol = "snpID",
chromosomeCol = "chromosome",
positionCol = "position",
alleleACol = "alleleA",
alleleBCol = "alleleB",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# SnpAnnotationReader
# Generic reader class
# Add more Reader classes as necessary
# NULL is included so GenotypeData, etc. are not required to have annotation
setClassUnion("SnpAnnotationReader", c("SnpAnnotationDataFrame",
"SnpAnnotationSQLite", "NULL"))
# ScanAnnotationDataFrame
# Scan Annotation stored as an AnnotatedDataFrame
setClass("ScanAnnotationDataFrame",
contains = "AnnotatedDataFrame",
representation(idCol = "character",
sexCol = "character"),
prototype(idCol = "scanID",
sexCol = "sex"))
# ScanAnnotationSQLite
# Scan Annotation stored in a SQLite database
setClass("ScanAnnotationSQLite",
representation(dbpath = "character",
dbcon = "SQLiteConnection",
annotationTable = "character",
metadataTable = "character",
idCol = "character",
sexCol = "character"),
prototype(idCol = "scanID",
sexCol = "sex"))
# ScanAnnotationReader
# Generic reader class
# Add more Reader classes as necessary
# NULL is included so GenotypeData, etc. are not required to have annotation
setClassUnion("ScanAnnotationReader", c("ScanAnnotationDataFrame",
"ScanAnnotationSQLite", "NULL"))
# NcdfReader
# Wrapper for the ncdf library - holds ncdf file handler
# ncdf is S3 class, so create S4 virtualization
setOldClass("ncdf4")
setClass("NcdfReader",
representation(filename = "character",
handler = "ncdf4"))
# NcdfGenotypeReader
# Reads genotype data stored in netCDF format
setClass("NcdfGenotypeReader",
contains = "NcdfReader",
representation(snpDim = "character",
scanDim = "character",
snpIDvar = "character",
chromosomeVar = "character",
positionVar = "character",
scanIDvar = "character",
genotypeVar = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(snpDim = "snp",
scanDim = "sample",
snpIDvar = "snp",
chromosomeVar = "chromosome",
positionVar = "position",
scanIDvar = "sampleID",
genotypeVar = "genotype",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# MatrixGenotypeReader
# Stores genotype data in a matrix
setClass("MatrixGenotypeReader",
representation(snpID = "integer",
chromosome = "integer",
position = "integer",
scanID = "integer",
genotype = "matrix",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# GdsReader
# holds GDS file handler (gdsfmt library)
setOldClass("gds.class")
setClass("GdsReader",
representation(filename = "character",
handler = "gds.class"))
# GdsGenotypeReader
# Reads genotype data stored in GDS format
setClass("GdsGenotypeReader",
contains = "GdsReader",
representation(snpIDvar = "character",
chromosomeVar = "character",
positionVar = "character",
scanIDvar = "character",
genotypeVar = "character",
alleleVar = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer",
genotypeDim = "character",
missingValue = "integer"),
prototype(snpIDvar = "snp.id",
chromosomeVar = "snp.chromosome",
positionVar = "snp.position",
scanIDvar = "sample.id",
genotypeVar = "genotype",
alleleVar = "snp.allele",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L,
genotypeDim = "",
missingValue = 3L))
# GenotypeReader
# Generic reader class
# Add more Reader classes as necessary
setClassUnion("GenotypeReader", c("NcdfGenotypeReader", "MatrixGenotypeReader",
"GdsGenotypeReader"))
# GenotypeData
setClass("GenotypeData",
representation(data = "GenotypeReader",
snpAnnot = "SnpAnnotationReader",
scanAnnot = "ScanAnnotationReader"),
prototype(snpAnnot = NULL,
scanAnnot = NULL))
# NcdfIntensityReader
# Reads intensity data stored in netCDF format
setClass("NcdfIntensityReader",
contains = "NcdfReader",
representation(snpDim = "character",
scanDim = "character",
snpIDvar = "character",
chromosomeVar = "character",
positionVar = "character",
scanIDvar = "character",
qualityVar = "character",
xVar = "character",
yVar = "character",
bafVar = "character",
lrrVar = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(snpDim = "snp",
scanDim = "sample",
snpIDvar = "snp",
chromosomeVar = "chromosome",
positionVar = "position",
scanIDvar = "sampleID",
qualityVar = "quality",
xVar = "X",
yVar = "Y",
bafVar = "BAlleleFreq",
lrrVar = "LogRRatio",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# GdsIntensityReader
# Reads intensity data stored in netCDF format
setClass("GdsIntensityReader",
contains = "GdsReader",
representation(snpDim = "character",
scanDim = "character",
snpIDvar = "character",
chromosomeVar = "character",
positionVar = "character",
scanIDvar = "character",
qualityVar = "character",
xVar = "character",
yVar = "character",
bafVar = "character",
lrrVar = "character",
autosomeCode = "integer",
XchromCode = "integer",
YchromCode = "integer",
XYchromCode = "integer",
MchromCode = "integer"),
prototype(snpIDvar = "snp.id",
chromosomeVar = "snp.chromosome",
positionVar = "snp.position",
scanIDvar = "sample.id",
qualityVar = "quality",
xVar = "X",
yVar = "Y",
bafVar = "BAlleleFreq",
lrrVar = "LogRRatio",
autosomeCode = 1:22,
XchromCode = 23L,
YchromCode = 25L,
XYchromCode = 24L,
MchromCode = 26L))
# IntensityReader
# Generic reader class
# Add more Reader classes as necessary
setClassUnion("IntensityReader", c("NcdfIntensityReader", "GdsIntensityReader"))
# IntensityData
setClass("IntensityData",
representation(data = "IntensityReader",
snpAnnot = "SnpAnnotationReader",
scanAnnot = "ScanAnnotationReader"),
prototype(snpAnnot = NULL,
scanAnnot = NULL))
# Iterator class
setClass("GenotypeIterator", contains="GenotypeData",
slots=c(snpFilter="list",
lastFilter="environment")) # allow pass-by-reference for this slot
# Block iterator
setClass("GenotypeBlockIterator", contains="GenotypeIterator",
slots=c(snpBlock="integer")) # number of snps
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