Facilitating genome annotation using ANNEXA and long-read RNA sequencing

With the advent of complete genome assemblies, genome annotation has become essential for the functional interpretation of genomic data. Long-read RNA sequencing (LR-RNAseq) technologies have significantly improved transcriptome annotation by enabling full-length transcript reconstruction for both coding and non-coding RNAs. However, challenges such as transcript fragmentation and incomplete isoform representation persist, highlighting the need for robust quality control (QC) strategies. This study presents an updated version of ANNEXA, a pipeline designed to enhance genome annotation using LR-RNAseq data while also providing QC for reconstructed genes and transcripts. ANNEXA integrates two transcriptome reconstruction tools, StringTie2 and Bambu, applying stringent filtering criteria to improve annotation accuracy. It also incorporates deep learning models to evaluate transcription start sites (TSSs) and employs the tool FEELnc for the systematic annotation of long non-coding RNAs (lncR-NAs). Additionally, the pipeline offers intuitive visualizations for comparative analyses of coding and non-coding repertoires. Benchmarking against multiple reference annotations revealed distinct patterns of sensitivity and precision for both known and novel genes and transcripts and mRNAs and lncRNAs. To demonstrate its utility, ANNEXA was applied in a comparative oncology study involving LR-RNAseq of two human and eight canine cancer cell lines. The pipeline successfully identified novel genes and transcripts across species, expanding the catalog of protein-coding and lncRNA annotations in both species. Implemented in Nextflow for scalability and reproducibility, AN-NEXA is available as an open-source tool: https://github.com/IGDRion/ANNEXA .