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