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Hannah Macpherson

dblp:430/0869 · DBLP profile ↗
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1ranked-venue papers
0as first author
1since 2021 · last 2026
—ORCID · unresolved

Domains — the database's venue-derived domains; a paper can count in several

Applied, interdisciplinary, general and emerging computing · 1 · 1 since 2021

Expertise — from the expertise taxonomy: the topics of the expert's papers under the CCF categories. A weight counts papers with recency: 1 for a paper about the topic, 0.3 when the topic is its context, halved every five years.

Interdisciplinary, comprehensive, and emerging computing
1 paper
Bioinformatics and computational biology · 100%

Topics — the 4 heaviest of 4, each with the papers that count most for it

TopicWeightPapersLastEvidence papers
Bioinformatics and computational biology › genome annotation › coding region prediction
open reading frame prediction
1.012026
ORFannotate: reproducible coding sequence annotation of transcriptome assemblies · Bioinform. 2026
Bioinformatics and computational biology › transcriptomics
transcriptome annotation
1.012026
ORFannotate: reproducible coding sequence annotation of transcriptome assemblies · Bioinform. 2026
Bioinformatics and computational biology › sequence analysis
long-read sequencing
0.312026
ORFannotate: reproducible coding sequence annotation of transcriptome assemblies · Bioinform. 2026
Bioinformatics and computational biology › sequence analysis › sequence assembly
transcriptome assembly
0.312026
ORFannotate: reproducible coding sequence annotation of transcriptome assemblies · Bioinform. 2026

Methods — techniques the papers use, named apart from their topics

kozak sequence analysis · 1.0NMD prediction · 1.0GTF-native annotation · 1.0
YearPublicationVenuePosition
2026 ORFannotate: reproducible coding sequence annotation of transcriptome assemblies
abstract
SUMMARY: Accurate 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).
Sonia García-Ruíz, Hannah Macpherson, Laura Caton, Mina Ryten, Emil K. Gustavsson
Bioinform.2