asSnpMatrix | R Documentation |
asSnpMatrix
converts a GenotypeData
object to a SnpMatrix-class
object.
asSnpMatrix(genoData, snpNames="snpID", scanNames="scanID",
snp=c(1,-1), scan=c(1,-1))
genoData |
A |
snpNames |
The name of the SNP variable in |
scanNames |
The name of the scan variable in |
snp |
An integer vector of the form (start, count), where start is the index of the first data element to read and count is the number of elements to read. A value of '-1' for count indicates that all SNPs should be read. |
scan |
An integer vector of the form (start, count), where start is the index of the first data element to read and count is the number of elements to read. A value of '-1' for count indicates that all scans should be read. |
The default is to extract all SNPs and scans from genoData
, but
for a large dataset this may exceed R's memory limit. Alternatively,
snp
and scan
may be used to specify (start,
count)
of SNPs and scans to extract from genoData
.
In the SnpMatrix
object, genotypes are stored as 0 = missing, 1
= "A/A", 2= "A/B" or "B/A", and 3 = "B/B". (In a GenotypeData
object, 0 = "B/B", 1 = "A/B" or "B/A", and 2 = "A/A".)
Columns are SNPs with
names snpNames
and rows are scans with names scanNames
(the transpose of the GenotypeData
object).
A SnpMatrix-class
object.
Stephanie Gogarten
SnpMatrix-class
, GenotypeData
library(snpStats)
library(GWASdata)
file <- system.file("extdata", "illumina_geno.gds", package="GWASdata")
gds <- GdsGenotypeReader(file)
data(illuminaSnpADF, illuminaScanADF)
genoData <- GenotypeData(gds, snpAnnot=illuminaSnpADF, scanAnnot=illuminaScanADF)
snpmat <- asSnpMatrix(genoData, snpNames="rsID", scanNames="scanID")
snpmat
as(snpmat[1:5, 1:5], "character")
summary(snpmat)
# only chromosome 21
chr <- getChromosome(genoData)
c21 <- which(chr == 21)
snpmat <- asSnpMatrix(genoData, snpNames="rsID", scanNames="scanID",
snp=c(c21[1], length(c21)))
snpmat
close(genoData)
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