bamSummarise | summarise mapping observations from a BAM file |
bamSummariseByChr | summarise mapping observations from a BAM file by chromosome |
bamSummaryToCoverage | get depth of coverage information from across the genome |
chromosomeMappingSummary | prepare mapping summary information by chromosome |
cleanReferenceGenome | cleanup the reference genome data |
fastqCheckup | perform a sanity check and prepare summary info on fastq file |
fastqValidator | parse a fastq file aiming to validate sequences |
fixFastq | fix a corrupted fastq file (if fastq-like) |
getChromosomeIds | get chromosome identifiers from reference genome |
getChromosomeSequence | returns a DNAStringSet object corresponding to specified chromosome from reference genome |
getFastqBases | return the number of fastq bases previously parsed from provided Fastq file |
getFastqCount | return the number of fastq entries previously parsed from provided Fastq file |
getFastqPlusErrorCount | count of fastq elements rejected due to line 3 plus separator |
getMalformedFastqHeaderCount | count of fastq elements rejected due to malformed fastq header |
getReferenceGenome | get path reference genome object |
getRpath | get path for R results |
getSeqLengths | get chromosome lengths for a named set of chromosomes |
getSequenceQualityMismatchCount | count of fastq elements rejected due to mismatch between sequence and quality field lengths |
getSkippedLineCount | count of lines of fastq file skipped to enable fastq entry parsing |
getStringSetId | accessory method for mapping named chromosomes to their pointers in the reference fasta |
getZeroLengthSequenceCount | count of fastq elements rejected due to zero length sequence |
infoGraphicPlot3 | prepare an 3x infographic-styled summary plot |
infoGraphicPlot4 | prepare a 4x infographic-styled summary plot |
init | Initialise the NanopoRe environment |
isInitialised | check NanopoRe environment |
lcalc | calculate Lstatistics (e.g. L50) for given sequence collection |
LeftRightPlot | plot two ggplot2 figures side by side |
listCachedObjects | Initialise the NanopoRe environment |
loadReferenceGenome | load reference genome into memory |
md5sum | calculate md5sum checksum for qualified file |
ncalc | calculate Nstatistics (e.g. N50) for given sequence collection |
parallelBamSummarise | summarise mapping observations from a BAM file using parallel chr-by-chr |
phredmean | calculate mean Phred scores from list of Q values |
plotAlignmentAccuracy | plot a histogram of mapping accuracies |
plotAlignmentIdentity | plot a histogram of mapping identities |
plotDepthOfCoverageMegablock | plot a tiled panel of chromosomal depths-of-coverage |
plotOverallCovHistogram | plot a histogram of whole genome depth-of-coverage |
qualToMeanQ | calculate mean Phred score from an ASCII encoded phred string |
setReferenceGenome | set path for reference genome object |
setRpath | set path for R results |
snifflesKaryogram | prepare karyogram of annotated SVs |
svLengthDistribution | prepare figure of SV length distribution |
testBam | extract content from a BAM file |
Vcf2FilteredGranges | extract SV variants from a sniffles VCF file by SVTYPE |
Vcf2GRanges | convert VCF content into a GRanges object for nanopoRe usage |