CrisprRun-class: CrisprRun class

Description Arguments Fields Methods Author(s) See Also Examples

Description

A ReferenceClass container for a single sample of alignments narrowed to a target region. Typically CrisprRun objects will not be accessed directly, but if necessary via a CrisprSet class which contains a list of CrisprRun objects. Note that the CrispRVariants plotting functions don't work on CrisprRun objects.

Arguments

bam

a GAlignments object containing (narrowed) alignments to the target region. Filtering of the bam should generally be done before initialising a CrisprRun object

target

The target location, a GRanges object

genome.ranges

A GRangesList of genomic coordinates for the cigar operations. If bam is a standard GAlignments object, this is equivalent to cigarRangesAlongReferenceSpace + start(bam)

rc

(reverse complement) Should the alignments be reverse complemented, i.e. displayed with respect to the negative strand? (Default: FALSE)

name

A name for this set of reads, used in plots if present (Default: NULL)

chimeras

Off-target chimeric alignments not in bam. (Default: empty)

verbose

Print information about initialisation progress (Default: FALSE)

Fields

alns

A GAlignments object containing the narrowed reads. Note that if the alignments are represented with respect to the reverse strand, the "start" remains with repect to the forward strand, whilst the cigar and the sequence are reverse complemented.

name

The name of the sample

cigar_labels

A vector of labels for the reads, based on the cigar strings, optionally renumbered with respect to a new zero point (e.g. the cut site) and shortened to only insertion and deletion locations. Set at initialisation of a CrisprSet object, but not at initialisation of a CrisprRun object.

chimeras

Chimeric, off-target alignments corresponding to alignments in alns

Methods

getCigarLabels(target, target.loc, genome_to_target, ref, separate.snv, rc, match.label, mismatch.label, keep.ops = c("I", "D", "N"), upstream = min(target.loc, 8), downstream = min(6, width(ref) - target.loc + 1), regions = NULL, snv.regions = NULL)

Description: Sets the "cig_labels" field, returns the cigar labels.

Input parameters: target: (GRanges) the counting region. target.loc: The location of the cut site with respect to the target genome_to_target: A vector with names being genomic locations and values being locations with respect to the cut site separate.snv: Should single nucleotide variants be called? (Default: TRUE) match.label: Label for non-variant reads (Default: no variant) mismatch.label: Label for single nucleotide variants (Default: SNV) rc: Should the variants be displayed with respect to the negative strand? (Default: FALSE) keep.ops: CIGAR operations to remain in the variant label (usually indels) upstream: distance upstream of the cut site to call SNVs downstream: distance downstream of the cut site to call SNVs regions: IRanges(k) Regions for counting insertions and deletions. Insertions on the right border are not counted. snv.regions Regions for calling SNVS

getInsertionSeqs(target)

Description: Return a table relating insertion sequences to alignment indices Input parameters:

Author(s)

Helen Lindsay

See Also

CrisprSet

Examples

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# readsToTarget with signature("GAlignments", "GRanges") returns a 
# CrisprRun object

bam_fname <- system.file("extdata", "gol_F1_clutch_1_embryo_1_s.bam",
                        package = "CrispRVariants")
param <- Rsamtools::ScanBamParam(what = c("seq", "flag"))
alns <- GenomicAlignments::readGAlignments(bam_fname, param = param, 
         use.names = TRUE)

reference <- Biostrings::DNAString("GGTCTCTCGCAGGATGTTGCTGG")
gd <- GenomicRanges::GRanges("18", IRanges::IRanges(4647377, 4647399), strand = "+")

crispr_run <- readsToTarget(alns, target = gd, reference = reference,
                           name = "Sample name", target.loc = 17)

# Alternatively, CrisprRun objects can be accessed from a CrisprSet object
# e.g. crispr_set$crispr_runs[[1]]

HLindsay/CrispRVariants documentation built on May 28, 2019, 12:40 p.m.