We have released a new version (1.0.5) of the Shannon splicing mutation pipeline.
The new version now processes large sets of variants (ie. from multiple complete genomes) more quickly, and now includes the ability to import variants using CLC bio’s variant track format (in addition to VCF).
Documentation has been significantly improved and several sets of example data are provided with the software release. The documentation contains additional screenshots of the expected input and output, and now includes a page providing tips on how to filter the output using CLC bio’s built in functionality.