Nothing
## ---- echo=FALSE--------------------------------------------------------------
knitr::opts_chunk$set(error=FALSE, warning=FALSE, message=FALSE)
library(BiocStyle)
## ---- eval=!exists("SCREENSHOT"), include=FALSE-------------------------------
SCREENSHOT <- function(x, ...) knitr::include_graphics(x)
## -----------------------------------------------------------------------------
library(iSEEu)
## -----------------------------------------------------------------------------
library(airway)
data(airway)
library(edgeR)
y <- DGEList(assay(airway), samples=colData(airway))
y <- y[filterByExpr(y, group=y$samples$dex),]
y <- calcNormFactors(y)
design <- model.matrix(~dex, y$samples)
y <- estimateDisp(y, design)
fit <- glmQLFit(y, design)
res <- glmQLFTest(fit, coef=2)
tab <- topTags(res, n=Inf)$table
rowData(airway) <- cbind(rowData(airway), tab[rownames(airway),])
## -----------------------------------------------------------------------------
ma.panel <- MAPlot(PanelWidth=6L)
app <- iSEE(airway, initial=list(ma.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/ma.png")
## -----------------------------------------------------------------------------
vol.panel <- VolcanoPlot(PanelWidth=6L)
app <- iSEE(airway, initial=list(vol.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/volcano.png")
## -----------------------------------------------------------------------------
# Creating another comparison, this time by blocking on the cell line
design.alt <- model.matrix(~cell + dex, y$samples)
y.alt <- estimateDisp(y, design.alt)
fit.alt <- glmQLFit(y.alt, design.alt)
res.alt <- glmQLFTest(fit.alt, coef=2)
tab.alt <- topTags(res.alt, n=Inf)$table
rowData(airway) <- cbind(rowData(airway), alt=tab.alt[rownames(airway),])
lfc.panel <- LogFCLogFCPlot(PanelWidth=6L, YAxis="alt.logFC",
YPValueField="alt.PValue")
app <- iSEE(airway, initial=list(lfc.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/logfclogfc.png")
## -----------------------------------------------------------------------------
library(scRNAseq)
sce <- ReprocessedAllenData(assays="tophat_counts")
library(scater)
sce <- logNormCounts(sce, exprs_values="tophat_counts")
sce <- runPCA(sce, ncomponents=4)
sce <- runTSNE(sce)
## -----------------------------------------------------------------------------
# Receives a selection from a reduced dimension plot.
dyn.panel <- DynamicReducedDimensionPlot(Type="UMAP", Assay="logcounts",
ColumnSelectionSource="ReducedDimensionPlot1", PanelWidth=6L)
# NOTE: users do not have to manually create this, just
# copy it from the "Panel Settings" of an already open app.
red.panel <- ReducedDimensionPlot(PanelId=1L, PanelWidth=6L,
BrushData = list(
xmin = -45.943, xmax = -15.399, ymin = -58.560,
ymax = 49.701, coords_css = list(xmin = 51.009,
xmax = 165.009, ymin = 39.009,
ymax = 422.009), coords_img = list(xmin = 66.313,
xmax = 214.514, ymin = 50.712,
ymax = 548.612), img_css_ratio = list(x = 1.300,
y = 1.299), mapping = list(x = "X", y = "Y"),
domain = list(left = -49.101, right = 57.228,
bottom = -70.389, top = 53.519),
range = list(left = 50.986, right = 566.922,
bottom = 603.013, top = 33.155),
log = list(x = NULL, y = NULL), direction = "xy",
brushId = "ReducedDimensionPlot1_Brush",
outputId = "ReducedDimensionPlot1"
)
)
app <- iSEE(sce, initial=list(red.panel, dyn.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/dynreddim.png")
## -----------------------------------------------------------------------------
diff.panel <- DynamicMarkerTable(PanelWidth=8L, Assay="logcounts",
ColumnSelectionSource="ReducedDimensionPlot1",)
# Recycling the reduced dimension panel above, adding a saved selection to
# compare to the active selection.
red.panel[["SelectionHistory"]] <- list(
BrushData = list(
xmin = 15.143, xmax = 57.228, ymin = -40.752,
ymax = 25.674, coords_css = list(xmin = 279.009,
xmax = 436.089, ymin = 124.009,
ymax = 359.009), coords_img = list(xmin = 362.716,
xmax = 566.922, ymin = 161.212,
ymax = 466.712), img_css_ratio = list(x = 1.300,
y = 1.299), mapping = list(x = "X", y = "Y"),
domain = list(left = -49.101, right = 57.228,
bottom = -70.389, top = 53.519),
range = list(left = 50.986, right = 566.922,
bottom = 603.013, top = 33.155),
log = list(x = NULL, y = NULL), direction = "xy",
brushId = "ReducedDimensionPlot1_Brush",
outputId = "ReducedDimensionPlot1"
)
)
red.panel[["PanelWidth"]] <- 4L # To fit onto one line.
app <- iSEE(sce, initial=list(red.panel, diff.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/diffstat.png")
## -----------------------------------------------------------------------------
setFeatureSetCommands(createGeneSetCommands(identifier="ENSEMBL"))
gset.tab <- FeatureSetTable(Selected="GO:0002576",
Search="platelet", PanelWidth=6L)
# This volcano plot will highlight the genes in the selected gene set.
vol.panel <- VolcanoPlot(RowSelectionSource="FeatureSetTable1",
SelectionEffect="Color", PanelWidth=6L)
app <- iSEE(airway, initial=list(gset.tab, vol.panel))
## ---- echo=FALSE--------------------------------------------------------------
SCREENSHOT("screenshots/geneset.png", delay=30)
## -----------------------------------------------------------------------------
sessionInfo()
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