API of GenomKit
- Genomic Sequences
- Genomic Alignments
- Genomic Regions
GRegionGRegionsGRegions.add()GRegions.close_regions()GRegions.cluster()GRegions.extend()GRegions.extend_fold()GRegions.filter_by_names()GRegions.filter_by_score()GRegions.get_GSequences()GRegions.get_names()GRegions.get_sequences()GRegions.intersect()GRegions.load()GRegions.merge()GRegions.remove_duplicates()GRegions.resize()GRegions.sampling()GRegions.sort()GRegions.split()GRegions.subtract()GRegions.total_coverage()GRegions.write()
GRegionsSet
- Genomic Annotation
- Genomic Coverages
GCoveragesGCoverages.calculate_coverage_GRegions()GCoverages.calculate_coverage_GRegions2()GCoverages.calculate_coverage_from_bam()GCoverages.filter_regions_coverage()GCoverages.flip_negative_regions()GCoverages.get_coverage()GCoverages.get_dataframe()GCoverages.load_coverage_from_bigwig()GCoverages.scale_coverage()GCoverages.total_sequencing_depth()
- Genomic Variants