Loci2path: regulatory annotation of genomic intervals based on

In loci2path: Loci2path: regulatory annotation of genomic intervals based on tissue-specific expression QTLs

Prepare input dataset for query

Query regions

loci2path takes query regions in the format of GenomicRanges. Only the Genomic Locations (chromosomes, start and end position) will be used. Strand information and other metadata columns are ignored. In the demo data, 47 regions associated with Psoriasis disease were downloaded from immunoBase.org and used as demo query regions.

require(GenomicRanges)
bed.file <- system.file("extdata", "query/Psoriasis.BED", package = "loci2path")
query.bed <- read.table(bed.file, header=FALSE)
colnames(query.bed) <- c("chr","start","end")
query.gr <- makeGRangesFromDataFrame(query.bed)

Prepare eQTL sets.

eQTL sets are entities recording 1-to-1 links between eQTL SNPs and genes. eQTL set entity also contains the following information: tissue name for the eQTL study, IDs and genomic ranges for the eQTL SNPs, IDs for the associated genes.

eQTL set can be constructed manually by specifying the corresponding information in each slot.

eQTL set list is a list of multiple eQTL sets, usually collected from different tissues.

Below is an example to construct customized eQTL set and eQTL set list using demo data files. In the demo data folder, three eQTL sets downloaded from GTEx project are included. Due to the large size, each eQTL dataset is down sampled to 3000 records for demostration purpose.

construct eQTL set

library(loci2path)
library(GenomicRanges)
brain.file <- system.file("extdata", "eqtl/brain.gtex.txt", 
                       package="loci2path")
tab <- read.table(brain.file, stringsAsFactors=FALSE, header=TRUE)
snp.gr <- GRanges(seqnames=Rle(tab$snp.chr), 
  ranges=IRanges(start=tab$snp.pos, 
  width=1))
brain.eset <- eqtlSet(tissue="brain",
  eqtlId=tab$snp.id,
  eqtlRange=snp.gr,
  gene=as.character(tab$gene.entrez.id))
brain.eset

skin.file <- system.file("extdata", "eqtl/skin.gtex.txt", package="loci2path")
tab=read.table(skin.file, stringsAsFactors=FALSE, header=TRUE)
snp.gr <- GRanges(seqnames=Rle(tab$snp.chr), 
  ranges=IRanges(start=tab$snp.pos, 
  width=1))
skin.eset <- eqtlSet(tissue="skin",
  eqtlId=tab$snp.id,
  eqtlRange=snp.gr,
  gene=as.character(tab$gene.entrez.id))
skin.eset

blood.file <- system.file("extdata", "eqtl/blood.gtex.txt", 
                       package="loci2path")
tab <- read.table(blood.file, stringsAsFactors=FALSE, header=TRUE)
snp.gr <- GRanges(seqnames=Rle(tab$snp.chr), 
  ranges=IRanges(start=tab$snp.pos, 
  width=1))
blood.eset <- eqtlSet(tissue="blood",
  eqtlId=tab$snp.id,
  eqtlRange=snp.gr,
  gene=as.character(tab$gene.entrez.id))
blood.eset

construct eQTL set list

eset.list <- list(Brain=brain.eset, Skin=skin.eset, Blood=blood.eset)
eset.list

Prepare gene set collection

A geneset collection contains a list of gene sets, with each gene set is represented as a vector of member genes. A vector of description is also provided as the metadata slot for each gene set. The total number of gene in the geneset collection is also required to perform the enrichment test. In this tutorial the BIOCARTA pathway collection was downloaded from MSigDB.

biocarta.link.file <- system.file("extdata", "geneSet/biocarta.txt", 
                               package="loci2path")
biocarta.set.file <- system.file("extdata", "geneSet/biocarta.set.txt", 
                              package="loci2path")

biocarta.link <- read.delim(biocarta.link.file, header=FALSE, 
                         stringsAsFactors=FALSE)
set.geneid <- read.table(biocarta.set.file, stringsAsFactors=FALSE)
set.geneid <- strsplit(set.geneid[,1], split=",")
names(set.geneid) <- biocarta.link[,1]

head(biocarta.link)
head(set.geneid)

In order to build gene set, we also need to know the total number of genes in order to perform enrichment test. In this study, the total number of gene in MSigDB pathway collection is 31,847[@Liberzon2015]

#build geneSet
biocarta <- geneSet(
    numGene=31847,
    description=biocarta.link[,2],
    geneSetList=set.geneid)
biocarta

Perform query

peroform query from one eQTL set

#query from one eQTL set.
res.one <- query(
  query.gr=query.gr,
  loci=skin.eset, 
  path=biocarta)

#enrichment result table
res.one$result.table

#all the genes associated with eQTLs covered by the query region
res.one$cover.gene

peroform query from multiple eQTL sets

#query from one eQTL set.
res.esetlist <- query(
  query.gr=query.gr, 
  loci=eset.list, 
  path=biocarta)  

#enrichment result table, tissue column added
resultTable(res.esetlist)

#all the genes associated with eQTLs covered by the query region; 
#names of the list are tissue names from eqtl set list
coveredGene(res.esetlist)

parallel query from multiple eQTL sets

#query from one eQTL set.
res.paral <- query(
  query.gr=query.gr, 
  loci=eset.list, 
  path=biocarta, 
  parallel=TRUE)  
#should return the same result as res.esetlist

explore query result

result <- resultTable(res.esetlist)

obtain eQTL gene list

#all the genes associated with eQTLs covered by the query region
res.one$cover.gene

#all the genes associated with eQTLs covered by the query region; 
#names of the list are tissue names from eqtl set list
coveredGene(res.esetlist)

obtain average tissue degree for each pathway

tissue.degree <- getTissueDegree(res.esetlist, eset.list)

#check gene-tissue mapping for each gene
head(tissue.degree$gene.tissue.map)

#check degree for each gene
head(tissue.degree$gene.tissue.degree)

#average tissue degree for the input result table
tissue.degree$mean.tissue.degree

#add avg. tissue degree to existing result table
res.tissue <- data.frame(resultTable(res.esetlist),
                      t.degree=tissue.degree$mean.tissue.degree)

obtain tissue enrichment for query regions

In this case, in the generic function \code{query}, only the argunment \code{loci} need to be provided. This will trigger the query of tissue specificity

#query tissue specificity
gr.tissue <- query(query.gr, loci=eset.list)
gr.tissue

extract tissue-pathway heatmap

#extract tissue-pathway matrix
mat <- getMat(res.esetlist, test.method="gene")

#plot heatmap
heatmap.para <- getHeatmap(res.esetlist)

extract word cloud from result

#plot word cloud
wc <- getWordcloud(res.esetlist)

plot p-value distribution of result

#plot p-value distribution of result
pval <- getPval(res.esetlist, test.method="gene")

obtain geneset description from object

#obtain geneset description from object
description <- getPathDescription(res.esetlist, biocarta)
head(description)

Session info

sessionInfo()

References

loci2path documentation built on Nov. 8, 2020, 6:08 p.m.