ClairS and Clair3-RNA

These two tools are complements within the RNA-structure-learning category, as ClairS is a general deep-learning method for somatic small variant calling from long reads, while Clair3-RNA is specifically designed as a long-read small variant caller tailored for RNA sequencing data, suggesting ClairS could be a foundational or related somatic variant caller that Clair3-RNA then adapts or extends for the nuances of RNA-seq.