* New feature: distinguish noncanonical and canonical novel splice sites for direct repeat hist * New feature: option to drop partially aligned reads with the min_align_fraction parameter in add_sample_from_bam
0.2.4
* New feature: added option to save read names during bam import * new feature: gzip compressed gtf output
0.2.3
* Changed assignment of transcripts to genes if no splice sites match. * Fix: more flexible import of reference files, gene name not required (but id is), introducing "infer_genes" from exon entries of gtf files. * New function: Transcriptome.remove_filter(filter=[tags])
0.2.2
* Fix: export to gtf with filter features
0.2.1
* Fix: import reference from gtf file * New feature: Import multiple samples from single bam tagged by barcode (e.g. from single cell data) * Fix: issue with zero base exons after shifting fuzzy junctions
0.2.0
* restructure to meet PyPI recommendations * New feature: isoseq.altsplice_test accepts more than 2 groups, and computes ML parameters for all groups