Oshlack / MINTIE Star 33 Code Issues Pull requests Method for Identifying Novel Transcripts and Isoforms using Equivalence classes, in cancer and rare disease. rna-seq cancer transcriptomics structural-variation duplications rare-disease gene-fusions cryptic-variants Updated Jul 1, 2024 Python
bcgsc / pavfinder Star 17 Code Issues Pull requests 🔍 Post Assembly Variants Finder bioinformatics rna-seq assembly structural-variants gene-fusions splice-variants Updated Oct 7, 2022 Python
skchronicles / RNA-seek Star 10 Code Issues Pull requests Discussions A comprehensive quality-control and quantification RNA-seq pipeline quality-control rna-seq gene-expression singularity gene-fusions snakemake-pipeline Updated Mar 27, 2024 Python