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.