1 Installation

As of Bioconductor 3.11 (release date April 28, 2020), BRGenomics can be installed directly from Bioconductor:

# install.packages("BiocManager")
BiocManager::install("BRGenomics")

Alternatively, the latest development version can be installed from
GitHub:

# install.packages("remotes")
remotes::install_github("mdeber/BRGenomics@R3")

BRGenomics (and Bioconductor 3.11) require R version 4.0 (release April 24, 2020). Installing the R3 branch, as shown above, is required to install under R 3.x.

If you install the development version from Github and you’re using Windows, Rtools for Windows is required.

2 Parallel Processing

By default, many BRGenomics functions use multicore processing as implemented in the parallel package. BRGenomics functions that can be parallelized always contain the argument ncores. If not specified, the default is to use the global option “mc.cores” (the same option used by the parallel package), or 2 if that option is not set.

If you wanted to change the global default to 4 cores, for example, you would run options(mc.cores = 4) at the start of your R session. If you’re unsure how many cores your processor has, run parallel::detectCores().

While performance can be memory constrained in some cases (and thus actually hampered by excessive parallelization), substantial performance benefits can be achieved by maximizing parallelization.

However, parallel processing is not available on Windows. To maintain compatibility, all code in this vignette as well as the example code in the documentation is to use a single core, i.e. ncores = 1.

3 Included Datasets

BRGenomics ships with an example dataset of PRO-seq data from Drosophila melanogaster1 Hojoong Kwak, Nicholas J. Fuda, Leighton J. Core, John T. Lis (2013). Precise Maps of RNA Polymerase Reveal How Promoters Direct Initiation and Pausing. Science 339(6122): 950–953. https://doi.org/10.1126/science.1229386. PRO-seq is a basepair-resolution method that uses 3’-end sequencing of nascent RNA to map the locations of actively engaged RNA polymerases.

To keep the dataset small, we’ve only included reads mapping to the fourth chromosome2 Chromosome 4 in Drosophila, often referred to as the “dot” chromosome, is very small and contains very few genes.

The included datasets can be accessed using the data() function:

library(BRGenomics)
data("PROseq")
PROseq
## GRanges object with 47380 ranges and 1 metadata column:
##           seqnames    ranges strand |     score
##              <Rle> <IRanges>  <Rle> | <integer>
##       [1]     chr4      1295      + |         1
##       [2]     chr4     41428      + |         1
##       [3]     chr4     42588      + |         1
##       [4]     chr4     42590      + |         2
##       [5]     chr4     42593      + |         5
##       ...      ...       ...    ... .       ...
##   [47376]     chr4   1307742      - |         1
##   [47377]     chr4   1316537      - |         1
##   [47378]     chr4   1318960      - |         1
##   [47379]     chr4   1319004      - |         1
##   [47380]     chr4   1319369      - |         1
##   -------
##   seqinfo: 7 sequences from an unspecified genome

Notice that the data is contained within a GRanges object. GRanges objects, from the GenomicRanges package, are very easy to work with, and are supported by a plethora of useful functions and packages.

The structure of the data will be described later on (in section “Basepair-Resolution GRanges Objects”). For now, we’ll just note that both annotations (e.g. genelists) and data are contained using the same GRanges class.

We’ve included an example genelist to accompany the PRO-seq data:

data("txs_dm6_chr4")
txs_dm6_chr4
## GRanges object with 339 ranges and 2 metadata columns:
##         seqnames          ranges strand |     tx_name     gene_id
##            <Rle>       <IRanges>  <Rle> | <character> <character>
##     [1]     chr4        879-5039      + | FBtr0346692 FBgn0267363
##     [2]     chr4     42774-43374      + | FBtr0344900 FBgn0266617
##     [3]     chr4     44774-46074      + | FBtr0340499 FBgn0265633
##     [4]     chr4     56497-60974      + | FBtr0333704 FBgn0264617
##     [5]     chr4     56497-63124      + | FBtr0333705 FBgn0264617
##     ...      ...             ...    ... .         ...         ...
##   [335]     chr4 1192419-1196848      - | FBtr0100543 FBgn0039924
##   [336]     chr4 1192419-1196848      - | FBtr0100544 FBgn0039924
##   [337]     chr4 1225089-1230713      - | FBtr0100406 FBgn0027101
##   [338]     chr4 1225737-1230713      - | FBtr0100402 FBgn0027101
##   [339]     chr4 1225737-1230713      - | FBtr0100404 FBgn0027101
##   -------
##   seqinfo: 7 sequences from dm6 genome

The GRanges above contains all Flybase annotated transcripts from chromosome 4, with no filtering of any kind.

4 Basic Operations on GRanges

For users who are unfamiliar with GRanges objects, this section demonstrates a number of basic operations.

A quick summary of the general structure: Each element of a GRanges object is called a “range”. As you can see above, each range consists of several components: seqnames, ranges, and strand. These essential attributes are all found to the left of the vertical divider above; everything to the right of that divider is an optional, metadata attribute.

The core attributes can be accessed using the functions seqnames(), ranges(), and strand(). All metadata can be accessed using mcols(), and individual columns are accessible with the $ operator. The only reserved metadata column is the score column, which is just like any other metadata column, except that users can use the score() function to assess it.

All of the above functions are both “getters” and “setters”, e.g. strand(x) returns the strand information, and strand(x) <- "+" assigns it.

These and other operations are demonstrated below.


To learn more about GRanges objects, including a general overview of their components, see the useful vignette An Introduction to the GenomicRanges Package. Alternatively, see the archived materials from the 2018 Bioconductor workshop Solving Common Bioinformatic Challenges Using GenomicRanges. Note that this package will implement and streamline a number of common operations, but users should still have a basic familiarity with GRanges objects.


 

Get the length of the genelist:

length(txs_dm6_chr4) 
## [1] 339

 

Select the 2nd transcript:

txs_dm6_chr4[2]
## GRanges object with 1 range and 2 metadata columns:
##       seqnames      ranges strand |     tx_name     gene_id
##          <Rle>   <IRanges>  <Rle> | <character> <character>
##   [1]     chr4 42774-43374      + | FBtr0344900 FBgn0266617
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Select 4 transcripts:

tx4 <- txs_dm6_chr4[c(1, 10, 200, 300)]
tx4
## GRanges object with 4 ranges and 2 metadata columns:
##       seqnames          ranges strand |     tx_name     gene_id
##          <Rle>       <IRanges>  <Rle> | <character> <character>
##   [1]     chr4        879-5039      + | FBtr0346692 FBgn0267363
##   [2]     chr4    69326-110059      + | FBtr0308615 FBgn0085432
##   [3]     chr4   184225-193489      - | FBtr0089150 FBgn0039890
##   [4]     chr4 1009895-1027101      - | FBtr0309865 FBgn0025741
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Get the lengths of the first 4 transcripts:

width(tx4)
## [1]  4161 40734  9265 17207

 

Get a dataframe of the metadata for the first 4 transcripts:

mcols(tx4)
## DataFrame with 4 rows and 2 columns
##       tx_name     gene_id
##   <character> <character>
## 1 FBtr0346692 FBgn0267363
## 2 FBtr0308615 FBgn0085432
## 3 FBtr0089150 FBgn0039890
## 4 FBtr0309865 FBgn0025741

 

Access a single metadata column for the first 4 transcripts:

mcols(tx4)[, 2]
## [1] "FBgn0267363" "FBgn0085432" "FBgn0039890" "FBgn0025741"
mcols(tx4)[, "gene_id"]
## [1] "FBgn0267363" "FBgn0085432" "FBgn0039890" "FBgn0025741"
tx4$gene_id
## [1] "FBgn0267363" "FBgn0085432" "FBgn0039890" "FBgn0025741"
tx4_names <- tx4$tx_name
tx4_names
## [1] "FBtr0346692" "FBtr0308615" "FBtr0089150" "FBtr0309865"

 

Get the first gene_id (a metadata element):

tx4$gene_id[1]
## [1] "FBgn0267363"

 

Remove a metadata column:

mcols(tx4) <- mcols(tx4)[, -1]
tx4
## GRanges object with 4 ranges and 1 metadata column:
##       seqnames          ranges strand |           X
##          <Rle>       <IRanges>  <Rle> | <character>
##   [1]     chr4        879-5039      + | FBgn0267363
##   [2]     chr4    69326-110059      + | FBgn0085432
##   [3]     chr4   184225-193489      - | FBgn0039890
##   [4]     chr4 1009895-1027101      - | FBgn0025741
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Rename metadata:

names(mcols(tx4)) <- "gene_id"
tx4
## GRanges object with 4 ranges and 1 metadata column:
##       seqnames          ranges strand |     gene_id
##          <Rle>       <IRanges>  <Rle> | <character>
##   [1]     chr4        879-5039      + | FBgn0267363
##   [2]     chr4    69326-110059      + | FBgn0085432
##   [3]     chr4   184225-193489      - | FBgn0039890
##   [4]     chr4 1009895-1027101      - | FBgn0025741
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Add metadata; same as access methods (mcols()[], mcols()$, or simply $):

tx4$tx_name <- tx4_names
tx4
## GRanges object with 4 ranges and 2 metadata columns:
##       seqnames          ranges strand |     gene_id     tx_name
##          <Rle>       <IRanges>  <Rle> | <character> <character>
##   [1]     chr4        879-5039      + | FBgn0267363 FBtr0346692
##   [2]     chr4    69326-110059      + | FBgn0085432 FBtr0308615
##   [3]     chr4   184225-193489      - | FBgn0039890 FBtr0089150
##   [4]     chr4 1009895-1027101      - | FBgn0025741 FBtr0309865
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Modify metadata:

tx4$gene_id[1] <- "gene1"
tx4$tx_name <- 1:4
tx4
## GRanges object with 4 ranges and 2 metadata columns:
##       seqnames          ranges strand |     gene_id   tx_name
##          <Rle>       <IRanges>  <Rle> | <character> <integer>
##   [1]     chr4        879-5039      + |       gene1         1
##   [2]     chr4    69326-110059      + | FBgn0085432         2
##   [3]     chr4   184225-193489      - | FBgn0039890         3
##   [4]     chr4 1009895-1027101      - | FBgn0025741         4
##   -------
##   seqinfo: 7 sequences from dm6 genome

 

Get beginning of ranges (not strand specific):

start(tx4)
## [1]     879   69326  184225 1009895

 

Get beginning of ranges (strand specific):

tx4_tss <- resize(tx4, width = 1, fix = "start")
tx4_tss
## GRanges object with 4 ranges and 2 metadata columns:
##       seqnames    ranges strand |     gene_id   tx_name
##          <Rle> <IRanges>  <Rle> | <character> <integer>
##   [1]     chr4       879      + |       gene1         1
##   [2]     chr4     69326      + | FBgn0085432         2
##   [3]     chr4    193489      - | FBgn0039890         3
##   [4]     chr4   1027101      - | FBgn0025741         4
##   -------
##   seqinfo: 7 sequences from dm6 genome
start(tx4_tss)
## [1]     879   69326  193489 1027101

 

Remove all metadata:

mcols(tx4) <- NULL
tx4
## GRanges object with 4 ranges and 0 metadata columns:
##       seqnames          ranges strand
##          <Rle>       <IRanges>  <Rle>
##   [1]     chr4        879-5039      +
##   [2]     chr4    69326-110059      +
##   [3]     chr4   184225-193489      -
##   [4]     chr4 1009895-1027101      -
##   -------
##   seqinfo: 7 sequences from dm6 genome