Nothing
## Correlation testing
context("test on correlation")
test_that("correlation computation is correct", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
inTadSig <- newSigInTAD(enhSel, enhSelGR, rpkmCountsSel, txsSel)
inTadSig <- combineInTAD(inTadSig, tadGR)
cID <- "chr15:26372163-26398073" #E2
corData <- findCorrelation(inTadSig)
selCorData <- corData[corData$peakid == cID, ]
expect_equal( nrow(selCorData) , 30 )
expect_equal( selCorData[ selCorData$name == "GABRA5","cor" ] , 0.878531,tolerance=1e-6)
# this gene should be in since option closest is active
expect_equal( selCorData[ selCorData$name == "GABRB3","cor" ] , 0.6304704, tolerance=1e-6)
})
test_that("correlation properties are working correctly", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
inTadSig <- newSigInTAD(enhSel, enhSelGR, rpkmCountsSel, txsSel)
inTadSig <- combineInTAD(inTadSig, tadGR)
corData <- findCorrelation(inTadSig, method="spearman")
cID <- "chr15:26372163-26398073" #E2
selCorData <- corData[corData$peakid == cID, ]
expect_equal( selCorData[ selCorData$name == "GABRA5","cor" ] , 0.8361538, tolerance=1e-6)
corData <- findCorrelation(inTadSig, adj.pval = TRUE)
expect_equal( ncol(corData) , 9)
selCorData <- corData[corData$peakid == cID, ]
expect_equal( selCorData[ selCorData$name == "GABRA5","qvalue" ] , 6.276324e-06, tolerance=1e-6)
# novel option 18.11.2018
expect_equal( selCorData[ selCorData$name == "GABRA5","eucDist" ] , 10.92154 , tolerance=1e-6)
})
test_that("combine intad options are working correctly", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
inTadSig <- newSigInTAD(enhSel, enhSelGR, rpkmCountsSel, txsSel)
inTadSig <- combineInTAD(inTadSig, tadGR, closestGene = FALSE)
corData <- findCorrelation(inTadSig)
cID <- "chr15:26372163-26398073" #E2
selCorData <- corData[corData$peakid == cID, ]
expect_equal( nrow(selCorData) , 13)
expect_equal( selCorData[ selCorData$name == "GABRA5","cor" ] , 0.878531,tolerance=1e-6)
})
test_that("check intad selMaxTadOvlp option", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
# adjust enhancers to initial selection
targ <- findOverlaps(enhSelGR, GRanges("chr15:26003055-26976587"))
enhSelGR <- enhSelGR[queryHits(targ)]
enhSel <- enhSel[as.character(enhSelGR),]
# novel enhnacer overlapping 2 tads
# std tad chr15:25728907-27128907, close tad chr15:23608559-25368907
novEnh <- "chr15:25367907-25738907"
enhSel2 <- rbind(enhSel, c(rep(1, 20),rep(2,5)))
rownames(enhSel2)[66] <- novEnh
enhSelGR2 <- c(enhSelGR,GRanges(novEnh))
inTadSig <- newSigInTAD(enhSel2, enhSelGR2, rpkmCountsSel, txsSel)
inTadSig <- filterGeneExpr(inTadSig, checkExprDistr = TRUE)
# combine genes and signals in TAD: default largest overlap
inTadSig <- combineInTAD(inTadSig, tadGR)
expect_equal( length(inTadSig@signalConnections[[novEnh]]$tad) , 8)
# combine enh with both TADs
inTadSig <- combineInTAD(inTadSig, tadGR,selMaxTadOvlp = FALSE)
expect_equal( length(inTadSig@signalConnections[[novEnh]]$tad) , 68)
})
test_that("check intad effect of no enhancers and TADs", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
# edit enhancers to remove overlap with TADs
enhSelGR2 <- enhSelGR[1:2]
start(enhSelGR2) <- c(3000,5000)
end(enhSelGR2) <- c(4000,6000)
inTadSig <- newSigInTAD(enhSel[1:2,], enhSelGR2, rpkmCountsSel, txsSel)
expect_that(combineInTAD(inTadSig, tadGR),
throws_error("No overlaps found between signal regions and TADs!"))
})
test_that("test loops usage", {
data("mbSelEnhSignals")
data("enhSelCoords")
data("mbSamplesRPKM")
data("txsSel")
inTadSig <- newSigInTAD(enhSel, enhSelGR, rpkmCountsSel, txsSel)
inTadSig <- combineWithLoops(inTadSig,loopsDfSel)
res <- findCorFromLoops(inTadSig,method = "spearman")
expect_equal( nrow(res) , 1)
expect_equal( res[ 1,"name" ] ,"GABRA5")
expect_equal( res[ 1,"cor" ] , 0.6123077,tolerance=1e-6)
})
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