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Record W4407957525 · doi:10.1038/s41586-025-08623-w

Rare disease gene association discovery in the 100,000 GenomesProject

2025· article· en· W4407957525 on OpenAlexaff
Valentina Cipriani, Letizia Vestito, Emma Magavern, Julius O.B. Jacobsen, Gavin Arno, Elijah R. Behr, Katherine A. Benson, Marta Bértoli, Detlef Böckenhauer, Michael R. Bowl, Kate Burley, Li F. Chan, Patrick F. Chinnery, Peter J. Conlon, Marcos Abreu Costa, Alice E. Davidson, Sally J. Dawson, Elhussein A. Elhassan, Sarah E. Flanagan, Marta Futema, Daniel P. Gale, Sonia García-Ruiz, M. Cecilia Gonzalez Corcia, Helen Griffin, Sophie Hambleton, Amy R. Hicks, Henry Houlden, Richard S. Houlston, Sarah Howles, Robert Kleta, Iris Lekkerkerker, Siying Lin, Petra Lišková, Hannah M. Mitchison, Heba Morsy, Andrew Mumford, William G. Newman, Ruxandra Neatu, Edel A. O’Toole, Albert Ong, Alistair T. Pagnamenta, Shamima Rahman, Neil Rajan, Peter N. Robinson, Mina Ryten, Omid Sadeghi‐Alavijeh, John A. Sayer, Claire L. Shovlin, Jenny C. Taylor, Omri Teltsh, Ian Tomlinson, Arianna Tucci, Clare Turnbull, Albertien M. van Eerde, James S. Ware, Laura Watts, Andrew R. Webster, Sarah K. Westbury, Sean L. Zheng, Mark J. Caulfield, Damian Smedley

Bibliographic record

VenueNature · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenomics and Rare Diseases
Canadian institutionsUniversité de MontréalMcGill UniversityCentre Hospitalier Universitaire Sainte-Justine
FundersNational Institute of Child Health and Human DevelopmentMedical Research CouncilGrantová Agentura České RepublikyManchester Biomedical Research CentreUniversity College London Hospitals NHS Foundation TrustNIHR Imperial Biomedical Research CentreMichael J. Fox Foundation for Parkinson's ResearchDepartment of Health and Social CareNational Institutes of HealthCancer Research UKWellcome TrustNational Institute for Health and Care Research
KeywordsDiseaseGenome-wide association studyGenetic associationBiologyGeneticsIn silicoGenomeGeneMendelian inheritanceComputational biologyGenomicsBioinformaticsMedicineSingle-nucleotide polymorphismGenotypePathology

Abstract

fetched live from OpenAlex

Abstract Up to 80% of rare disease patients remain undiagnosed after genomic sequencing 1 , with many probably involving pathogenic variants in yet to be discovered disease–gene associations. To search for such associations, we developed a rare variant gene burden analytical framework for Mendelian diseases, and applied it to protein-coding variants from whole-genome sequencing of 34,851 cases and their family members recruited to the 100,000 Genomes Project 2 . A total of 141 new associations were identified, including five for which independent disease–gene evidence was recently published. Following in silico triaging and clinical expert review, 69 associations were prioritized, of which 30 could be linked to existing experimental evidence. The five associations with strongest overall genetic and experimental evidence were monogenic diabetes with the known β cell regulator 3,4 UNC13A , schizophrenia with GPR17 , epilepsy with RBFOX3 , Charcot–Marie–Tooth disease with ARPC3 and anterior segment ocular abnormalities with POMK . Further confirmation of these and other associations could lead to numerous diagnoses, highlighting the clinical impact of large-scale statistical approaches to rare disease–gene association discovery.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.014
metaresearch head score (Gemma)0.032
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: none
Teacher disagreement score0.014
Threshold uncertainty score0.072

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0140.032
Meta-epidemiology (narrow)0.0010.001
Meta-epidemiology (broad)0.0020.002
Bibliometrics0.0050.006
Science and technology studies0.0010.001
Scholarly communication0.0030.001
Open science0.0010.004
Research integrity0.0020.002
Insufficient payload (model declined to judge)0.0060.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.003
GPT teacher head0.244
Teacher spread0.240 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations17
Published2025
Admission routes1
Has abstractyes

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