knitr::opts_chunk$set(echo = TRUE)
library(Homo.sapiens) library(scRNAseq) library(scater) library(iSEEu.epiviz)
# Example dataset sce <- ReprocessedAllenData(assays="tophat_counts") set.seed(100) sce <- logNormCounts(sce, exprs_values="tophat_counts") sce <- runPCA(sce, ncomponents=4) sce <- runTSNE(sce) sce
data("tcga_colon_blocks") data("tcga_colon_expression")
browser <- EpivizBrowser(chr="chr11", start=118000000, end=121000000, genome=Homo.sapiens, tracks=list("tcga_peaks" = tcga_colon_blocks, "tcga_expression"=tcga_colon_expression), PanelWidth=12L, PanelHeight=400L)
app <- iSEE(sce, initial=list( ReducedDimensionPlot(Type="TSNE", VisualBoxOpen=TRUE, VisualChoices="Size", PanelWidth=6L), browser)) app
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