--- title: The iSEEhex package author: - name: Kevin Rue-Albrecht affiliation: - &id1 MRC Weatherall Institute of Molecular Medicine, University of Oxford, Headington, Oxford OX3 9DS, UK. email: kevin.rue-albrecht@imm.ox.ac.uk - name: Federico Marini affiliation: - &id2 Institute of Medical Biostatistics, Epidemiology and Informatics (IMBEI), Mainz - Center for Thrombosis and Hemostasis (CTH), Mainz email: marinif@uni-mainz.de - name: Charlotte Soneson affiliation: - &id3 Friedrich Miescher Institute for Biomedical Research, Basel - SIB Swiss Institute of Bioinformatics email: charlottesoneson@gmail.com - name: Aaron Lun email: infinite.monkeys.with.keyboards@gmail.com date: "`r BiocStyle::doc_date()`" package: iSEEhex output: BiocStyle::html_document vignette: > %\VignetteIndexEntry{Panel universe} %\VignetteEncoding{UTF-8} %\VignettePackage{iSEEhex} %\VignetteKeywords{GeneExpression, RNASeq, Sequencing, Visualization, QualityControl, GUI} %\VignetteEngine{knitr::rmarkdown} bibliography: iSEEhex.bib --- ```{r, echo=FALSE} knitr::opts_chunk$set( error=FALSE, warning=FALSE, message=FALSE, out.width='100%') library(BiocStyle) ``` ```{r, eval=!exists("SCREENSHOT"), include=FALSE} SCREENSHOT <- function(x, ...) knitr::include_graphics(x) ``` # Overview The `r Biocpkg("iSEE")` package [@iSEE-2018] provides a general and flexible framework for interactively exploring `SummarizedExperiment` objects. However, in many cases, more specialized panels are required for effective visualization of specific data types. The `r Biocpkg("iSEEhex")` package implements panels summarising data points in hexagonal bins, that work directly in the `iSEE` application and can smoothly interact with other panels. We first load in the package: ```{r} library(iSEEhex) ``` All the panels described in this document can be deployed by simply passing them into the `iSEE()` function via the `initial=` argument, as shown in the following examples. ## Example Let us prepare an example `r BiocStyle::Biocpkg("SingleCellExperiment")` object. ```{r} library(scRNAseq) # Example data ---- sce <- ReprocessedAllenData(assays="tophat_counts") class(sce) library(scater) sce <- logNormCounts(sce, exprs_values="tophat_counts") sce <- runPCA(sce, ncomponents=4) sce <- runTSNE(sce) rowData(sce)$ave_count <- rowMeans(assay(sce, "tophat_counts")) rowData(sce)$n_cells <- rowSums(assay(sce, "tophat_counts") > 0) sce ``` Then, we create an `r BiocStyle::Biocpkg("iSEE")` app that compares the `ReducedDimensionHexPlot` panel -- defined in this package -- to the standard `ReducedDimensionPlot` defined in the `r BiocStyle::Biocpkg("iSEE")` package. ```{r} initialPanels <- list( ReducedDimensionPlot( ColorBy = "Feature name", ColorByFeatureName = "Cux2", PanelWidth = 6L), ReducedDimensionHexPlot( ColorBy = "Feature name", ColorByFeatureName = "Cux2", PanelWidth = 6L, BinResolution = 30) ) app <- iSEE(se = sce, initial = initialPanels) ``` ```{r, echo=FALSE} SCREENSHOT("screenshots/reduced-dimension-hex-plot.png") ``` ## Further reading #### Where can I find a comprehensive introduction to `r Biocpkg("iSEE")`? {-} The `r Biocpkg("iSEE")` package contains several vignettes detailing the main functionality. You can also take a look at this [workshop](https://iSEE.github.io/iSEEWorkshop2019/index.html). A compiled version from the Bioc2019 conference (based on Bioconductor release 3.10) is available [here](http://biocworkshops2019.bioconductor.org.s3-website-us-east-1.amazonaws.com/page/iSEEWorkshop2019__iSEE-lab/). # Session information {-} ```{r} sessionInfo() ``` # References {-}