Evidence map›Paper›PMID 41702377›Full record

ArticleBioinformatics (Oxford, England)2026

ORFannotate: reproducible coding sequence annotation of transcriptome assemblies.

Sonia García-Ruiz, Hannah Macpherson, Laura Caton, Mina Ryten, Emil K Gustavsson

Abstract read
In one paragraph

Article in Bioinformatics (Oxford, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sonia García-RuizUK Dementia Research Institute, University of Cambridge, Cambridge, UK.ORCID 0000-0003-4913-5312
Hannah MacphersonDepartment of Neurodegenerative Disease, Queen Square Institute of Neurology, UCL, London, UK.
Laura CatonDepartment of Neurodegenerative Disease, Queen Square Institute of Neurology, UCL, London, UK.
Mina RytenUK Dementia Research Institute, University of Cambridge, Cambridge, UK.ORCID 0000-0001-9520-6957
Emil K GustavssonUK Dementia Research Institute, University of Cambridge, Cambridge, UK.ORCID 0000-0003-0541-7537

Funding

BrightFocus Foundation A2021009FTenure Track Clinician Scientist Fellowship MR/N008324/1
6 · The paper itself

Abstract

summaryAccurate annotation of coding sequences and translational features within transcript models is essential for interpreting assembled transcriptomes and their functional potential. Existing open reading frame (ORF) prediction tools typically operate on transcript FASTA files and do not reintegrate coding sequence (CDS) information back into transcript models, limiting their utility in long-read sequencing workflows where GTF/GFF annotations are the primary output. We present ORFannotate, a lightweight, GTF-native Python command-line tool that predicts ORFs from transcript annotations and reinserts precise, exon-aware CDS and UTR features into the original GTF/GFF file. In addition, ORFannotate provides biologically informative translational context by annotating Kozak sequence strength, detecting non-overlapping upstream ORFs (uORFs) with coding probabilities, characterising 5' and 3' untranslated regions (UTRs), and predicting nonsense-mediated decay (NMD) susceptibility. All annotations are consolidated in a transcript-level summary to support downstream analysis. By generating GTF files with accurate CDS annotations, ORFannotate facilitates reproducible analysis of both long- and short-read transcriptomes and integrates seamlessly with visualization tools, genome browsers, and comparative transcript analysis workflows. ORFannotate is fast, scalable and provides a practical solution for transcriptome annotation beyond coding potential prediction alone. AVAILABILITY AND IMPLEMENTATION: ORFannotate is implemented in Python and freely available under the GNU General Public License v3 (GPL-3.0) at: https://github.com/egustavsson/ORFannotate (DOI: https://doi.org/10.5281/zenodo.16812866).

Indexed as

Molecular Sequence AnnotationOpen Reading FramesSoftwareTranscriptome

Identifiers

PMID41702377
PMCPMC12960903

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.