BSgenome-class: BSgenome objects

In Przemol/mirrors-bioc-BSgenome: Infrastructure for Biostrings-based genome data packages

Description

The BSgenome class is a container for storing the full genome sequences of a given organism.

Accessor methods

In the code snippets below, x is a BSgenome object. Note that, because the BSgenome class contains the GenomeDescription class, then all the accessor methods for GenomeDescription objects can also be used on x.

sourceUrl(x)

Returns the source URL i.e. the permanent URL to the place where the FASTA files used to produce the sequences contained in x can be found (and downloaded).

seqnames(x), seqnames(x) <- value

Gets or sets the names of the single sequences contained in x. Each single sequence is stored in a DNAString or MaskedDNAString object and typically comes from a source file (FASTA) with a single record. The names returned by seqnames(x) usually reflect the names of those source files but a common prefix or suffix was eventually removed in order to keep them as short as possible.

seqlengths(x)

Returns the lengths of the single sequences contained in x.

See ?`length,XVector-method` and ?`length,MaskedXString-method` for the definition of the length of a DNAString or MaskedDNAString object. Note that the length of a masked sequence (MaskedXString object) is not affected by the current set of active masks but the nchar method for MaskedXString objects is.

names(seqlengths(x)) is guaranteed to be identical to seqnames(x).

mseqnames(x)

Returns the index of the multiple sequences contained in x. Each multiple sequence is stored in a DNAStringSet object and typically comes from a source file (FASTA) with multiple records. The names returned by mseqnames(x) usually reflect the names of those source files but a common prefix or suffix was eventually removed in order to keep them as short as possible.

names(x)

Returns the index of all sequences contained in x. This is the same as c(seqnames(x), mseqnames(x)).

length(x)

Returns the length of x, i.e., the total number of sequences in it (single and multiple sequences). This is the same as length(names(x)).

x[[name]]

Returns the sequence (single or multiple) in x named name (name must be a single string). No sequence is actually loaded into memory until this is explicitely requested with a call to x[[name]] or x$name. When loaded, a sequence is kept in a cache. It will be automatically removed from the cache at garbage collection if it's not in use anymore i.e. if there are no reference to it (other than the reference stored in the cache). With options(verbose=TRUE), a message is printed each time a sequence is removed from the cache.

x$name

Same as x[[name]] but name is not evaluated and therefore must be a literal character string or a name (possibly backtick quoted).

masknames(x)

The names of the built-in masks that are defined for all the single sequences. There can be up to 4 built-in masks per sequence. These will always be (in this order): (1) the mask of assembly gaps, aka "the AGAPS mask";

(2) the mask of intra-contig ambiguities, aka "the AMB mask";

(3) the mask of repeat regions that were determined by the RepeatMasker software, aka "the RM mask";

(4) the mask of repeat regions that were determined by the Tandem Repeats Finder software (where only repeats with period less than or equal to 12 were kept), aka "the TRF mask".

All the single sequences in a given package are guaranteed to have the same collection of built-in masks (same number of masks and in the same order).

masknames(x) gives the names of the masks in this collection. Therefore the value returned by masknames(x) is a character vector made of the first N elements of c("AGAPS", "AMB", "RM", "TRF"), where N depends only on the BSgenome data package being looked at (0 <= N <= 4). The man page for most BSgenome data packages should provide the exact list and permanent URLs of the source data files that were used to extract the built-in masks. For example, if you've installed the BSgenome.Hsapiens.UCSC.hg19 package, load it and see the Note section in ?`BSgenome.Hsapiens.UCSC.hg19`.

Author(s)

H. Pages

See Also

available.genomes, GenomeDescription-class, BSgenome-utils, DNAString-class, DNAStringSet-class, MaskedDNAString-class, getSeq,BSgenome-method, injectSNPs, subseq,XVector-method, rm, gc

Examples

## Loading a BSgenome data package doesn't load its sequences
## into memory:
library(BSgenome.Celegans.UCSC.ce2)

## Number of sequences in this genome:
length(Celegans) 

## Display a summary of the sequences:
Celegans

## Index of single sequences:
seqnames(Celegans)

## Lengths (i.e. number of nucleotides) of the single sequences:
seqlengths(Celegans)

## Load chromosome I from disk to memory (hence takes some time)
## and keep a reference to it:
chrI <- Celegans[["chrI"]]  # equivalent to Celegans$chrI

chrI

class(chrI)   # a DNAString instance
length(chrI)  # with 15080483 nucleotides

## Single sequence can be renamed:
seqnames(Celegans) <- sub("^chr", "", seqnames(Celegans))
seqlengths(Celegans)
Celegans$I
seqnames(Celegans) <- paste0("chr", seqnames(Celegans))

## Multiple sequences:
mseqnames(Celegans) 
upstream1000 <- Celegans$upstream1000
upstream1000
class(upstream1000)  # a DNAStringSet instance
## Character vector containing the description lines of the first
## 4 sequences in the original FASTA file:
names(upstream1000)[1:4]

## ---------------------------------------------------------------------
## PASS-BY-ADDRESS SEMANTIC, CACHING AND MEMORY USAGE
## ---------------------------------------------------------------------

## We want a message to be printed each time a sequence is removed
## from the cache:
options(verbose=TRUE)

gc()  # nothing seems to be removed from the cache
rm(chrI, upstream1000)
gc()  # chrI and upstream1000 are removed from the cache (they are
      # not in use anymore)

options(verbose=FALSE)

## Get the current amount of data in memory (in Mb):
mem0 <- gc()["Vcells", "(Mb)"]

system.time(chrV <- Celegans[["chrV"]])  # read from disk
  
gc()["Vcells", "(Mb)"] - mem0  # chrV occupies 20Mb in memory

system.time(tmp <- Celegans[["chrV"]])  # much faster! (sequence
                                        # is in the cache)

gc()["Vcells", "(Mb)"] - mem0  # we're still using 20Mb (sequences
                               # have a pass-by-address semantic
                               # i.e. the sequence data are not
                               # duplicated)
  
## subseq() doesn't copy the sequence data either, hence it is very
## fast and memory efficient (but the returned object will hold a
## reference to chrV):
y <- subseq(chrV, 10, 8000000) 
gc()["Vcells", "(Mb)"] - mem0

## We must remove all references to chrV before it can be removed from
## the cache (so the 20Mb of memory used by this sequence are freed).
options(verbose=TRUE)
rm(chrV, tmp)
gc()

## Remember that 'y' holds a reference to chrV too:
rm(y)
gc()

options(verbose=FALSE)
gc()["Vcells", "(Mb)"] - mem0

Przemol/mirrors-bioc-BSgenome documentation built on May 8, 2019, 3:46 a.m.