Abstract
Ribonucleic acids (RNAs) fold into complex structures that are strongly associated with their biological functions. These can be abstracted into secondary structures, represented as nucleotide sequences annotated with base-pairing information. This abstraction is both biologically relevant and computationally manageable. Comparing and classifying RNA molecules typically relies on these secondary structure representations, which exist in multiple formats. In this work, we introduce TARNAS 1.0, a software tool designed to convert RNA secondary structure representations across multiple formats, including Base Pair Sequence (BPSEQ), Connect Table (CT), dot-bracket, Arc-Annotated Sequence (AAS), Fast-All (FASTA), and RNA Markup Language (RNAML). The tool offers options for retaining or removing comments, blank lines, and headers during the conversion process. These format translation and preprocessing capabilities are specifically designed to support the batch handling of large collections of RNA molecules, making TARNAS well suited for large dataset construction and database curation. Beyond format translation, TARNAS computes three levels of abstraction for RNA secondary structures, namely core, core plus, and shape, as well as a set of statistical descriptors for both primary and secondary structure. These abstraction and analysis features are intended to facilitate the comparison of molecules and the identification of recurring structural patterns, which are essential steps for associating structural motifs with molecular function. TARNAS is available as both a standalone desktop application and a web-based tool. The desktop version supports batch processing of large datasets, while the web version is optimized for the analysis of single molecules.