---
title: "Introduction: a simple demo"
author: "Paul Shannon"
package: igvR
date: "`r Sys.Date()`"
output:
   BiocStyle::html_document
vignette: >
  %\VignetteIndexEntry{"Introduction: a simple demo"}
  %\VignetteEngine{knitr::rmarkdown}
  %\VignetteEncoding{UTF-8}
---

<style>
.main-container { width: 1200px; max-width:2800px;}
</style>


```{r setup, include = FALSE}
options(width=120)
knitr::opts_chunk$set(
   collapse = TRUE,
   eval=interactive(),
   echo=TRUE,
   comment = "#>"
)
```


# Overview

The igvR package provides easy programmatic access in R to the web-based javascript library
[igv.js](https://github.com/igvteam/igv.js) to create and display genome tracks in its richly
interactive web browser visual interface.

In this vignette we present a few very simple uses of igvR:

  - connect to the web browser
  - query the names (e.g., "mm10") of the currently supported genoems
  - specify that we will use the hg38 genome
  - zoom to the MYC gene
  - construct a simple data.frame specifying a bed-like track
  - display that data.frame track in the browser using a random color
  - create and display a "quantitative" data.frame
  - zoom out for a wider view

Your display will look like this at the conclusion of this demo:

```{r, eval=TRUE, echo=FALSE}
knitr::include_graphics("igvR-basicDemo.png")
```

# Load the libraries we need

```{r loadLibraries,  results='hide'}
library(igvR)
```

Create the igvR instance, with all default parameters (portRange, quiet, title).  Javascript and HTML is loaded into
your browser, igv.js is initialized, a websocket connection between your R process and that web page is constructed,
over which subsequent commands and data will travel.

```{r createLoad, results='hide'}
igv <- igvR()
setBrowserWindowTitle(igv, "simple igvR demo")
setGenome(igv, "hg38")
```

# Display a list of the currently supported genomes
```{r genomes, echo=TRUE, results='asis'}
print(getSupportedGenomes(igv))
```



# Display MYC
```{r initialDisplay,  results='hide'}
showGenomicRegion(igv, "MYC")
```

# Create and display  minimal 1-row data.frame centered below MYC on chr8

```{r simple data.frame,  results='hide'}
loc <- getGenomicRegion(igv)

tbl.bed <- data.frame(chrom=loc$chrom, start=loc$start + 2000, end=loc$end-2000,
                      name="simple.example", stringsAsFactors=FALSE)

track <- DataFrameAnnotationTrack("simple bed", tbl.bed, color="random")
displayTrack(igv, track)
```

# Create and display a simulated quantitative (bedGraph) track

```{r bedgraph-like data.frame,  results='hide'}
loc <- getGenomicRegion(igv)
size <- with(loc, 1 + end - start)
starts <- seq(loc$start, loc$end, by=5)
ends   <- starts + 5
values <- sample(1:100, size=length(starts), replace=TRUE)

tbl.bedGraph <- data.frame(chrom=rep("chr8", length(starts)), start=starts, end=ends,
                           value=values, stringsAsFactors=FALSE)

track <- DataFrameQuantitativeTrack("bedGraph", tbl.bedGraph, color="red", autoscale=FALSE,
                                    min=80, max=100)
displayTrack(igv, track)

```
# Zoom out by direct manipulation of the currently displayed region

```{r zoom out,  results='hide'}
loc <- getGenomicRegion(igv)
half.span <- round((loc$end-loc$start)/2)

new.region <- with(loc, sprintf("%s:%d-%d", chrom, start-half.span, end+half.span))
showGenomicRegion(igv, new.region)
```

# Zoom out and by function calls

```{r zoom out new,  results='hide'}

zoomOut(igv)
zoomIn(igv)
```


# Session Info

```{r sessionInfo}
sessionInfo()
```

