Description Usage Format Value Source Examples
Subsets of raw data available in this package and saved as Rdata objects for faster loading.
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counts
is a data frame with subset of counts from TrQuantCount_CEU_chr19.tsv
gene_ranges
is a GRanges object containing subset of gene coordinates from genes_chr19.bed
genotypes
is a data frame with subset of genotypes from genotypes_CEU_chr19.tsv
snp_ranges
is a Granges object containing subset of SNP coordinates from genotypes_CEU_chr19.tsv
For all the details on how these data sets were produced, see examples.
counts
, gene_ranges
, genotypes
, snp_ranges
Lappalainen T, Sammeth M, Friedlander MR, et al. Transcriptome and genome sequencing uncovers functional variation in humans. Nature. 2013;501(7468):506-11
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27 28 | library(rtracklayer)
data_dir <- system.file("extdata", package = "GeuvadisTranscriptExpr")
gene_id_subset <- readLines(file.path(data_dir, "gene_id_subset.txt"))
snp_id_subset <- readLines(file.path(data_dir, "snp_id_subset.txt"))
# Load gene ranges with names!
gene_ranges <- import(file.path(data_dir, "genes_chr19.bed"))
names(gene_ranges) <- mcols(gene_ranges)$name
gene_ranges <- gene_ranges[gene_id_subset, ]
# Load transcript counts
counts <- read.table(file.path(data_dir, "TrQuantCount_CEU_chr19.tsv"),
header = TRUE, sep = "\t", as.is = TRUE)
counts <- counts[counts$Gene_Symbol %in% gene_id_subset, ]
# Load genotypes
genotypes <- read.table(file.path(data_dir, "genotypes_CEU_chr19.tsv"),
header = TRUE, sep = "\t", as.is = TRUE)
genotypes <- genotypes[genotypes$snpId %in% snp_id_subset, ]
# Create SNP ranges with names!
snp_ranges <- GRanges(Rle(genotypes$chr), IRanges(genotypes$start,
genotypes$end))
names(snp_ranges) <- genotypes$snpId
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