Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation

Accurate gene annotations are fundamental for interpreting genetic variation, cellular function, and disease mechanisms. However, current human gene annotations are largely derived from transcriptomic data of individuals with European ancestry, leaving gaps of annotation that remain uncharacterized. Here, we generate over 800 million full-length reads with long-read RNA-seq in 43 lymphoblastoid cell line samples from eight genetically-diverse human populations and build a cross-ancestry gene annotation. We demonstrate that transcripts from non-European samples are underrepresented in reference gene annotations, leading to incomplete characterization in allele-specific transcript usage. Furthermore, we show that personal genome assemblies enhance transcript discovery compared to the generic GRCh38 reference assembly, even though genomic regions unique to each individual are heavily depleted of genes. These findings underscore the urgent need for a more inclusive gene annotation framework that accurately represents global transcriptome diversity.

Authors

Institutions

Publication Details

Journal
Nature Communications
Published
2025-12-03
DOI
https://doi.org/10.1038/s41467-025-66096-x
Citations
2
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
3.63

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation

Emilio Palumbo, Carme Arnan, Winona Oliveros, Roderic Guigó et al.
2 citations
Nature Communications
Genetic Associations and Epidemiology
3.63
article

Long-read transcriptomics of a diverse human cohort reveals ancestry bias in gene annotation

Emilio Palumbo, Carme Arnan, Winona Oliveros, Roderic Guigó, Sílvia Carbonell Sala, Fairlie Reese, Marta Melé, Fabien Degalez, Tamara Perteghella, Pau Clavell-Revelles
article en
2 citations

Abstract

Accurate gene annotations are fundamental for interpreting genetic variation, cellular function, and disease mechanisms. However, current human gene annotations are largely derived from transcriptomic data of individuals with European ancestry, leaving gaps of annotation that remain uncharacterized. Here, we generate over 800 million full-length reads with long-read RNA-seq in 43 lymphoblastoid cell line samples from eight genetically-diverse human populations and build a cross-ancestry gene annotation. We demonstrate that transcripts from non-European samples are underrepresented in reference gene annotations, leading to incomplete characterization in allele-specific transcript usage. Furthermore, we show that personal genome assemblies enhance transcript discovery compared to the generic GRCh38 reference assembly, even though genomic regions unique to each individual are heavily depleted of genes. These findings underscore the urgent need for a more inclusive gene annotation framework that accurately represents global transcriptome diversity.

Nature CommunicationsVol. 16(1)
Universitat Pompeu Fabra (ES), Barcelona Supercomputing Center (ES), Centre for Genomic Regulation (ES), Universitat de Barcelona (ES), Universitat Politècnica de Catalunya (ES)
California Institute of Technology, Fundació la Marató de TV3, Wellcome Trust, European Molecular Biology Laboratory, Ministerio de Ciencia, Innovación y Universidades, Centres de Recerca de Catalunya, Centre de Regulació Genòmica, European Commission, Generalitat de Catalunya, Ministerio de Ciencia e Innovación, Universitat de Barcelona, Barcelona Supercomputing Center, National Institutes of Health, Agencia Estatal de Investigación, European Social Fund
Openalex Percentile: Top 6%
Genetic Associations and Epidemiology
3.63
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.