LoRTIA Plus: a chemistry-agnostic, feature-first software package for long-read transcriptome annotation
Gábor TormaiD, Zsolt BalázsiD, Ádám FülöpiD, Dóra TombácziD, Zsolt BoldogkőiiD
Abstract
Long-read RNA sequencing (lrRNA-seq) enables direct reconstruction of full-length transcripts, yet existing annotation tools show variable performance across genomes and library chemistries, particularly for novel isoforms. We present LoRTIA Plus, a chemistry-agnostic suite for transcriptome annotation and reconstruction from lrRNA-seq data. LoRTIA Plus first detects and filters transcription start sites (TSSs), transcription end sites (TESs), and introns using adapter-aware and quality-based criteria, and evaluates read support before assembling high-confidence transcript models. We benchmarked LoRTIA Plus against bambu, FLAIR, IsoQuant, and NAGATA on KSHV transcriptomes with dense overlap, using a validated literature-supported boundary set, and on transcriptomes from three human cell lines from the Long Read RNA-seq Genome Annotation Assessment Project (LRGASP) sequenced with five long-read chemistries. On KSHV, LoRTIA Plus achieved the highest F1 scores for TSSs, TESs, and transcripts in both direct-cDNA and direct-RNA datasets by improving recall without sacrificing precision. Across human datasets, LoRTIA Plus consistently ranked among the top boundary annotators across all chemistries and was the best-performing tool in PCR-based libraries, while remaining highly competitive on native RNA. Junction- and isoform-level analyses show that LoRTIA Plus yields a rich, reproducible repertoire of novel isoforms and transcript boundaries from viral to human transcriptomes.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Facilitating genome annotation using ANNEXA and long-read RNA sequencing
Nicolaï Hoffmann, Aurore Besson, … Thomas Derrien·bioRxiv·Apr 16, 2025
- Systematic assessment of long-read RNA-seq methods for transcript identification and quantification
Francisco J. Pardo-Palacios, Dingjie Wang, … Angela Norie Brooks·Nature MethodsPeer-reviewed·Jun 7, 2024
- PeakLocus: A transcript-aware toolkit for RNA-Centric Genomic Annotation
George Boateng-Sarfo, Shashank Pritam, Sarah A. Signor·bioRxiv·Oct 19, 2026
- SQANTI3: curation of long-read transcriptomes for accurate identification of known and novel isoforms
Francisco J. Pardo-Palacios, Ángeles Arzalluz-Luque, … Ana Conesa·Nature MethodsPeer-reviewed·Mar 20, 2024
- Impact of sequencing technologies on long non-coding RNA computational identification
Alisson Gaspar Chiquitto, Lucas Otávio L. Silva, … Alexandre Rossi Paschoal·IEEE International Conference on Bioinformatics and Biomedicine (BIBM)Peer-reviewed·Dec 6, 2022
- Boosting Transcript Assembly via Delineating Transcript Start and End Sites
Irtesam Mahmud Khan, Xiaofei Carl Zang, … Mingfu Shao·bioRxiv·Oct 13, 2025