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Record W7074225190

Copy Number Variants Are Ovarian Cancer Risk Alleles at Known and Novel Risk Loci.

2022· article· en· W7074225190 on OpenAlexfundno aff

Bibliographic record

VenueApollo (University of Cambridge) · 2022
Typearticle
Languageen
FieldPhysics and Astronomy
TopicPhotorefractive and Nonlinear Optics
Canadian institutionsnot available
FundersMedical Research and Materiel CommandNational Center for Advancing Translational SciencesNational Institute of General Medical SciencesUniversity College LondonPeter MacCallum FoundationNational Cancer InstituteNational Health and Medical Research CouncilMedical Research CouncilNational Institutes of HealthHellenic Health FoundationInstitut Gustave-RoussyKræftens BekæmpelseCancer Council VictoriaDeutsche KrebshilfeCanadian Institutes of Health ResearchCancerfondenInstitut National de la Santé et de la Recherche MédicaleEuropean CommissionRoswell Park Cancer InstituteNational Institute for Health and Care ResearchAssociazione Italiana per la Ricerca sul CancroCancer Research UKU.S. Department of DefenseRadboud UniversiteitLon V. Smith FoundationUniversity of CambridgeFred C. and Katherine B. Andersen FoundationOvarian Cancer Research FundBundesministerium für Bildung und ForschungOvarian Cancer AustraliaSwedish Cancer FoundationWorld Cancer Research FundWellcome TrustPomorski Uniwersytet Medyczny W SzczecinieLigue Contre le CancerVanderbilt University Medical CenterDeutsches KrebsforschungszentrumMayo Foundation for Medical Education and ResearchMinnesota Ovarian Cancer AllianceMoffitt Cancer CenterVanderbilt UniversityUniversity of PittsburghNordForskVetenskapsrådetGeorgia Clinical and Translational Science AllianceOak FoundationCancer AustraliaPfizerInstituto de Salud Carlos IIIAmgen
KeywordsCopy-number variationOvarian cancerAlleleOdds ratioSingle-nucleotide polymorphismGenetic associationGenome-wide association studyPopulation
DOInot available

Abstract

fetched live from OpenAlex

BACKGROUND: Known risk alleles for epithelial ovarian cancer (EOC) account for approximately 40% of the heritability for EOC. Copy number variants (CNVs) have not been investigated as EOC risk alleles in a large population cohort. METHODS: Single nucleotide polymorphism array data from 13 071 EOC cases and 17 306 controls of White European ancestry were used to identify CNVs associated with EOC risk using a rare admixture maximum likelihood test for gene burden and a by-probe ratio test. We performed enrichment analysis of CNVs at known EOC risk loci and functional biofeatures in ovarian cancer-related cell types. RESULTS: We identified statistically significant risk associations with CNVs at known EOC risk genes; BRCA1 (PEOC = 1.60E-21; OREOC = 8.24), RAD51C (Phigh-grade serous ovarian cancer [HGSOC] = 5.5E-4; odds ratio [OR]HGSOC = 5.74 del), and BRCA2 (PHGSOC = 7.0E-4; ORHGSOC = 3.31 deletion). Four suggestive associations (P < .001) were identified for rare CNVs. Risk-associated CNVs were enriched (P < .05) at known EOC risk loci identified by genome-wide association study. Noncoding CNVs were enriched in active promoters and insulators in EOC-related cell types. CONCLUSIONS: CNVs in BRCA1 have been previously reported in smaller studies, but their observed frequency in this large population-based cohort, along with the CNVs observed at BRCA2 and RAD51C gene loci in EOC cases, suggests that these CNVs are potentially pathogenic and may contribute to the spectrum of disease-causing mutations in these genes. CNVs are likely to occur in a wider set of susceptibility regions, with potential implications for clinical genetic testing and disease prevention.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesInsufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.243
Threshold uncertainty score0.999

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.009
GPT teacher head0.216
Teacher spread0.207 · 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 teacher head, not a consensus.

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

Citations0
Published2022
Admission routes1
Has abstractyes

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