I’m currently using MAJIQ to detect local splicing variations, including novel junctions and cryptic exons, in a disease-focused mouse RNA-seq dataset.
Do the authors of MAJIQ or community members have any recommended approaches, tools, or best practices for transcript-level reconstruction from MAJIQ outputs? Specifically, I’m looking for a way to "stitch" novel junctions into transcript models, ideally in a way that maintains compatibility with existing annotations (Ensembl GRCm39). I'm looking to generate the predicted nucleotide sequences for the novel splice changes.
Cheers, Phillip