nch-igm/VarRNA: Initial release - v1.0.0

This is the first release of VarRNA, which accompanies the manuscript submission titled "Variant calling from RNA-Seq data reveals allele-specific differential expression of pathogenic cancer variants". Features include:

• RNA-Seq data processing (STAR alignment, GATK variant calling);
• Feature annotation with ANNOVAR; and
• Our model to classify variants as germline, somatic, or artifact.