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Record W4283079528 · doi:10.1101/2022.06.17.22276537

Exome sequencing identifies novel susceptibility genes and defines the contribution of coding variants to breast cancer risk

2022· preprint· en· W4283079528 on OpenAlexafffund
Naomi Wilcox, Martine Dumont, Anna González‐Neira, Sara Carvalho, Charles Joly Beauparlant, Marco Crotti, Craig Luccarini, Penny Soucy, Stéphane Dubois, Rocío Núñez‐Torres, Guillermo Pita, M. Rosario Alonso, Núria Álvarez, Caroline Baynes, Heiko Becher, Sabine Behrens, Manjeet K. Bolla, Jose E. Castelao, Jenny Chang‐Claude, Sten Cornelissen, Joe Dennis, Thilo Dörk, Christoph Engel, Manuela Gago-Domínguez, Pascal Guénel, Andreas Hadjisavvas, Eric Hahnen, Mikael Hartman, Belén Herráez, Audrey Jung, Renske Keeman, Marion Kiechle, Jingmei Li, Maria A. Loizidou, Michael Lush, Kyriaki Michailidou, Mihalis I. Panayiotidis, Xueling Sim, Soo‐Hwang Teo, Jonathan P. Tyrer, Lizet E. van der Kolk, Cecilia Wahlström, Qin Wang, Javier Benı́tez, Marjanka K. Schmidt, Rita K. Schmutzler, Paul D.P. Pharoah, Arnaud Droit, Alison M. Dunning, Anders Kvist, Peter Devilee, Douglas F. Easton, Jacques Simard

Bibliographic record

VenuemedRxiv · 2022
Typepreprint
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicBRCA gene mutations in cancer
Canadian institutionsUniversité LavalCentre hospitalier universitaire de Québec
FundersMedical Research CouncilEuropean CommissionFondation du cancer du sein du QuébecNational Cancer InstituteNational Institutes of HealthGovernment of CanadaWellcome TrustCanadian Institutes of Health ResearchGenome Canada
KeywordsPALB2CHEK2Missense mutationExome sequencingGeneticsExomeGeneBreast cancerBiologyGermline mutationMutationCancer

Abstract

fetched live from OpenAlex

Introductory paragraph Linkage and candidate gene studies have identified several breast cancer susceptibility genes, but the overall contribution of coding variation to breast cancer is unclear. To evaluate the role of rare coding variants more comprehensively, we performed a meta-analysis across three large whole-exome sequencing datasets, containing 16,498 cases and 182,142 controls. Burden tests were performed for protein-truncating and rare missense variants in 16,562 and 18,681 genes respectively. Associations between protein-truncating variants and breast cancer were identified for 7 genes at exome-wide significance ( P <2.5×10 -6 ): the five known susceptibility genes BRCA1, BRCA2, CHEK2, PALB2 and ATM , together with novel associations for ATRIP and MAP3K1 . Predicted deleterious rare missense or protein-truncating variants were additionally associated at P <2.5×10 -6 for SAMHD1 . The overall contribution of coding variants in genes beyond the previously known genes is estimated to be small.

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)0.001
metaresearch head score (Gemma)0.003
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: Empirical
Teacher disagreement score0.014
Threshold uncertainty score0.046

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0010.000
Open science0.0000.000
Research integrity0.0000.001
Insufficient payload (model declined to judge)0.0140.001

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 head0.024
GPT teacher head0.293
Teacher spread0.270 · 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

Citations1
Published2022
Admission routes2
Has abstractyes

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Same venuemedRxiv→Same topicBRCA gene mutations in cancer→French-language works237,207→