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Users can add transcriptomes from different datasets and explore distinct splicing and expression patterns across datasets.\n\nPlease visit the [Swan repository](https://github.com/mortazavilab/swan_vis) to download and view the source code\n\nAlso see the [Swan manuscript repository](https://github.com/fairliereese/swan_paper) for the exact commands used to do the analysis in our [publication](https://academic.oup.com/bioinformatics/advance-article/doi/10.1093/bioinformatics/btaa836/5912931).\n\nAlso see our [website](https://freese.gitbook.io/swan/) for in-depth tutorials and documentation\n\n## What can Swan do?\n\nSwan can make informative plots, find differentially expressed genes and transcripts, find isoform-switching genes, and discover novel exon skipping and intron retention events.\n\n## Installation\n\nSwan can be installed directly from PyPi. 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