TY - JOUR
T1 - An expanded reference catalog of translated open reading frames for biomedical research
AU - Chothani, Sonia
AU - Ruiz-Orera, Jorge
AU - Tierney, Jack A.S.
AU - Swirski, Michal I.
AU - Tjeldnes, Hakon
AU - Kok, Leron W.
AU - Clauwaert, Jim
AU - Deutsch, Eric W.
AU - Alba, M. Mar
AU - Aspden, Julie L.
AU - Baranov, Pavel V.
AU - Bazzini, Ariel Alejandro
AU - Bruford, Elspeth A.
AU - Brunet, Marie A.
AU - Cardon, Tristan
AU - Carvunis, Anne Ruxandra
AU - Casola, Claudio
AU - Choudhary, Jyoti Sharma S.
AU - Dean, Kellie
AU - Faridi, Pouya
AU - Fierro-Monti, Ivo
AU - Fournier, Isabelle
AU - Frankish, Adam
AU - Gerstein, Mark
AU - Hubner, Norbert
AU - Jiang, Yunzhe
AU - Kellis, Manolis
AU - Martinez, Thomas F.
AU - Menschaert, Gerben
AU - Ni, Pengyu
AU - Orchard, Sandra
AU - Roucou, Xavier
AU - Rozowsky, Joel
AU - Salzet, Michel
AU - Siragusa, Mauro
AU - Slavoff, Sarah
AU - Ternette, Nicola
AU - Vizcaino, Juan Antonio
AU - Wacholder, Aaron
AU - Wu, Wei
AU - Xie, Zhi
AU - Yang, Yucheng T.
AU - Moritz, Robert L.
AU - Valen, Eivind
AU - Mudge, Jonathan
AU - van Heesch, Sebastiaan
AU - Prensner, John R.
AU - Rackham, Owen J J.L.
N1 - © The Author(s) 2026. Published by Oxford University Press.
PY - 2026/4/13
Y1 - 2026/4/13
N2 - Non-canonical (i.e. unannotated) open reading frames (ncORFs) have until recently been omitted from reference genome annotations, despite evidence of their translation, limiting their incorporation into biomedical research. To address this, in 2022, we initiated the TransCODE consortium and built the first community-driven consensus catalog of human ncORFs, which was openly distributed to the research community via Ensembl-GENCODE. While this catalog represented a starting point for reference ncORF annotation, major technical and scientific issues remained. In particular, this initial catalog had no standardized framework to judge the evidence of translation for individual ncORFs. Here, we present an expanded and refined catalog of the human reference annotation of ncORFs. By incorporating more datasets and by lifting constraints on ORF length and start codon, we define a comprehensive set of 28 359 ncORFs that is nearly four times the size of the previous catalog. Furthermore, to aid users who wish to work with ncORFs with the strongest and most reproducible signals of translation, we utilized a data-driven framework (i.e. translation signature scores) to assess the accumulated evidence for any individual ncORF. Using this approach, we derive a subset of 10 127 ncORFs with translation evidence on par with canonical protein-coding genes, which we refer to as the primary set. This set can serve as a reliable reference for downstream analyses and validation, with a particular emphasis on high quality. Overall, this update reflects continuous community-driven efforts to make ncORFs accessible and actionable to the broader research public, and further iterations of the catalog will continue to expand and refine this resource.
AB - Non-canonical (i.e. unannotated) open reading frames (ncORFs) have until recently been omitted from reference genome annotations, despite evidence of their translation, limiting their incorporation into biomedical research. To address this, in 2022, we initiated the TransCODE consortium and built the first community-driven consensus catalog of human ncORFs, which was openly distributed to the research community via Ensembl-GENCODE. While this catalog represented a starting point for reference ncORF annotation, major technical and scientific issues remained. In particular, this initial catalog had no standardized framework to judge the evidence of translation for individual ncORFs. Here, we present an expanded and refined catalog of the human reference annotation of ncORFs. By incorporating more datasets and by lifting constraints on ORF length and start codon, we define a comprehensive set of 28 359 ncORFs that is nearly four times the size of the previous catalog. Furthermore, to aid users who wish to work with ncORFs with the strongest and most reproducible signals of translation, we utilized a data-driven framework (i.e. translation signature scores) to assess the accumulated evidence for any individual ncORF. Using this approach, we derive a subset of 10 127 ncORFs with translation evidence on par with canonical protein-coding genes, which we refer to as the primary set. This set can serve as a reliable reference for downstream analyses and validation, with a particular emphasis on high quality. Overall, this update reflects continuous community-driven efforts to make ncORFs accessible and actionable to the broader research public, and further iterations of the catalog will continue to expand and refine this resource.
KW - Protein Biosynthesis
KW - Humans
KW - Molecular Sequence Annotation
KW - Open Reading Frames/genetics
KW - Databases, Genetic
KW - Biomedical Research
KW - Genome, Human
UR - https://www.scopus.com/pages/publications/105034227642
U2 - 10.1093/nar/gkag234
DO - 10.1093/nar/gkag234
M3 - Article
C2 - 41873765
AN - SCOPUS:105034227642
SN - 0305-1048
VL - 54
JO - Nucleic acids research
JF - Nucleic acids research
IS - 6
ER -