install.packages('rbamtools')
"bamReader"
: Representation for file connection to BAM
file for reading access."bamHeader"
: Textual representation of header section
of BAM files."bamRange"
: Representation of genomic alignments in
defined regions.getNextAlign
: Retrieving next align from bamReader or bamRange"gapSiteList"
: Representation of genomic alignment gap
positions."gapList"
: Representation of genomic alignment gaps.getHeaderText
Assembling member data into Header-Text"geneAlignDepth"
: Align-depth data for single genes
on multiple samples (BAM files).filename
from bamReader or bamWriterbamAlign
and bamRange
"refSeqDict"
: Repesentation of data from reference
sequence dictionary in BAM file header."sampleBamFiles"
: Data on multiple BAM files from
an experimental setting."bamWriter"
: Representation of a file connection to
a BAM file for writing access."exonAlignDepth"
: Align-depth data for single genes
on multiple samples (BAM files). Intronic regions are cut out
of align depth matrix."exonLoessModel"
: Align-depth data for single genes
on multiple samples (BAM files). Intronic regions are cut out
of align depth matrix."headerLine"
: Representation of header line segment of
header section for BAM files."headerProgram"
: Represention of header - program section
of BAM header."headerReadGroup"
: Representation of read - group data
in header section of BAM files"rangeSegCount"
: Represents alignment counts in
segments of genetic regions."alignDepth"
: Alignment depth information from bamRange
objects."GenomePartition"
: ."bamAlign"
: Representation of single genomic alignments."bamGapList"
"bamHeader"
: Representation of data contained in the
header section of BAM files.