There are 5 repositories under alternative-splicing topic.
Lightweight and Fast; RNA-seq quantification at the event-level
AltAnalyze is a multi-functional and easy-to-use software package for automated single-cell and bulk gene and splicing analyses. Easy-to-use precompiled graphical user-interface versions available from our website.
Interactive R package to quantify, analyse and visualise alternative splicing
An RNA-Seq data exploration tool that shows read map coverage of a gene of interest along with a coloured "electronic fluorescent pictographic" (eFP) based on its RPKM expression level.
Use Thor's Axe to cut exons into their evolutionary building blocks :zap:
Baltica: integrated differential junction usage
Tutorials for using BRIE
Reproducibility of "Alternative start and termination sites of transcription drive most transcript isoform differences across human tissues."
A tool to model the evolution and structural impact of alternative splicing
A snakemake workflow to perform Alternative Splicing analysis from RNA-Seq with SUPPA2.
Computational biology pipeline that quantifies RNA splicing and performs sQTL mapping
The package RNAseqAnalysis does the complete analysis of RNA seq data starting from raw reads. It provides the user with differnt functions like generation of qc report, filtering, assembly and GO-term annotation, differential expression analysis and heatmap generation, and Alternative splicing-site prediction
IsoAligner: dynamic mapping of amino acid positions across protein isoforms
A supervised methodology for analyzing dysregulation in splicing machinery: an application in cancer diagnosis.
Docker to run rMATS for splicing quantification and analysis
SimSpliceEvol: Alternative splicing-aware simulation of biological sequence evolution
Quantification and Visualization of Variations of Splicing in Population
Functional impact of cancer-specific isoform switching events: Visualization via STRING interaction network
Method for retrieving and visualising the protein domains of any protein coding isoform and of different genomes. Enables joint visualisations representing alternative splicing events.