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Record W2509259734 · doi:10.1038/srep32512

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs)

2016· article· en· W2509259734 on OpenAlexafffund
Hatef Darabi, Jonathan Beesley, Arnaud Droit, Siddhartha Kar, Silje Nord, Mahdi Moradi Marjaneh, Penny Soucy, Kyriaki Michailidou, Maya Ghoussaini, Hanna Fues Wahl, Manjeet K. Bolla, Joe Dennis, M. Rosario Alonso, Irene L. Andrulis, Hoda Anton‐Culver, Volker Arndt, Matthias W. Beckmann, Javier Benı́tez, Natalia Bogdanova, Stig E. Bojesen, Hiltrud Brauch, Hermann Brenner, Annegien Broeks, Thomas Brüning, Barbara Burwinkel, Jenny Chang‐Claude, Ji‐Yeob Choi, Don Conroy, Fergus J. Couch, Angela Cox, Simon S. Cross, Kamila Czene, Peter Devilee, Thilo Dörk, Douglas F. Easton, Peter A. Fasching, Jonine D. Figueroa, Olivia Fletcher, Henrik Flyger, Eva Galle, Montserrat García‐Closas, Graham G. Giles, Mark S. Goldberg, Anna González‐Neira, Pascal Guénel, Christopher A. Haiman, Emily Hallberg, Ute Hamann, Mikael Hartman, Antoinette Hollestelle, John L. Hopper, Hidemi Ito, Anna Jakubowska, Nichola Johnson, Daehee Kang, Sofia Khan, Veli‐Matti Kosma, Mieke Kriege, Vessela Kristensen, Diether Lambrechts, Loı̈c Le Marchand, Soo Chin Lee, Annika Lindblom, Artitaya Lophatananon, Jan Lubiński, Siranoush Manoukian, Sara Margolin, Keitaro Matsuo, Rebecca Mayes, James McKay, Alfons Meindl, Roger L. Milne, Kenneth Muir, Susan L. Neuhausen, Heli Nevanlinna, Curtis Olswold, Nick Orr, Paolo Peterlongo, Guillermo Pita, Katri Pylkäs, Anja Rudolph, Suleeporn Sangrajrang, Elinor J. Sawyer, Marjanka K. Schmidt, Rita K. Schmutzler, Caroline Seynaeve, Mitul Shah, Chen‐Yang Shen, Xiao‐Ou Shu, Melissa C. Southey, Daniel O. Stram, Harald Surowy, Anthony J. Swerdlow, Soo‐Hwang Teo, Daniel C. Tessier, Ian Tomlinson, Diana Torres, Thérèse Truong, Celine M. Vachon, Daniel Vincent, Robert Winqvist, Anna H. Wu, Pei‐Ei Wu, Cheng Har Yip, Wei Zheng, Paul D.P. Pharoah, Per Hall, Stacey L. Edwards, Jacques Simard, Juliet D. French, Georgia Chenevix‐Trench, Alison M. Dunning

Bibliographic record

VenueScientific Reports · 2016
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer Genomics and Diagnostics
Canadian institutionsMcGill University and Génome Québec Innovation CentreMcGill UniversityRoyal Victoria HospitalUniversity of TorontoLunenfeld-Tanenbaum Research InstituteMount Sinai HospitalUniversité LavalCentre hospitalier universitaire de Québec
FundersMedical Research and Materiel CommandInstitute of Biomedical Sciences, Academia SinicaBiomedical Research CouncilMedical Research CouncilU.S. ArmyNational Institutes of HealthMinistero dello Sviluppo EconomicoAgence Nationale de Sécurité Sanitaire de l’Alimentation, de l’Environnement et du TravailCenters for Disease Control and PreventionInstitut National Du CancerNational Health and Medical Research CouncilOulun YliopistoDeutsche KrebshilfeMedizinischen Hochschule HannoverNorges ForskningsrådKWF KankerbestrijdingAssociazione Italiana per la Ricerca sul CancroMinistry of Public HealthLigue Contre le CancerKarolinska InstitutetInstituto de Salud Carlos IIINational Research Foundation of KoreaNational Medical Research CouncilMinistério da Ciência, Tecnologia e InovaçãoMinistry of Education, Science and TechnologyMinistry of Education, Culture, Sports, Science and TechnologyOvarian Cancer Research FundBundesministerium für Bildung und ForschungMinisterio de Economía y CompetitividadCanadian Institutes of Health ResearchGeneral Secretariat for Research and TechnologyRobert Bosch StiftungKementerian Sains, Teknologi dan InovasiKing's College LondonAcademy of FinlandAgence Nationale de la RechercheCancer Council South AustraliaFonds Wetenschappelijk OnderzoekCancerfondenStockholms Läns LandstingSingapore Eye Research InstituteNational Cancer InstituteCancer Institute NSWNational Breast Cancer FoundationEuropean CommissionKuopion Yliopistollinen SairaalaAcademia SinicaNational Research FoundationNational Institute for Health and Care ResearchBreast Cancer Research TrustFondation du cancer du sein du QuébecItä-Suomen YliopistoMinistère du Développement Économique, de l’Innovation et de l’ExportationLon V. Smith FoundationEuropean Social FundAgency for Science, Technology and ResearchCancer Council TasmaniaWorld Health OrganizationFrancis Crick InstituteNederlandse Organisatie voor Wetenschappelijk OnderzoekDeutsche Gesetzliche UnfallversicherungKreftforeningenDavid F. and Margaret T. Grohne Family FoundationBreast Cancer Research FoundationMcGill UniversityJapan Agency for Medical Research and DevelopmentDeutsches KrebsforschungszentrumHerlev HospitalCancer Research UKCancer Council NSWSusan G. Komen for the CureVirginia Department of HealthTaiwan BiobankCancer Council VictoriaCalifornia Department of Public HealthSundhed og Sygdom, Det Frie ForskningsrådFondation de FranceCalifornia Breast Cancer Research ProgramNIHR Biomedical Research Centre, Royal Marsden NHS Foundation Trust/Institute of Cancer ResearchU.S. Department of Health and Human ServicesUniversity of CambridgeHelsingin ja Uudenmaan Sairaanhoitopiiri
KeywordsSingle-nucleotide polymorphismBreast cancerLocus (genetics)GeneticsBiologyGeneComputational biologyBioinformaticsCancerMedicineGenotype

Abstract

fetched live from OpenAlex

Genome-wide association studies have found SNPs at 17q22 to be associated with breast cancer risk. To identify potential causal variants related to breast cancer risk, we performed a high resolution fine-mapping analysis that involved genotyping 517 SNPs using a custom Illumina iSelect array (iCOGS) followed by imputation of genotypes for 3,134 SNPs in more than 89,000 participants of European ancestry from the Breast Cancer Association Consortium (BCAC). We identified 28 highly correlated common variants, in a 53 Kb region spanning two introns of the STXBP4 gene, that are strong candidates for driving breast cancer risk (lead SNP rs2787486 (OR = 0.92; CI 0.90-0.94; P = 8.96 × 10(-15))) and are correlated with two previously reported risk-associated variants at this locus, SNPs rs6504950 (OR = 0.94, P = 2.04 × 10(-09), r(2) = 0.73 with lead SNP) and rs1156287 (OR = 0.93, P = 3.41 × 10(-11), r(2) = 0.83 with lead SNP). Analyses indicate only one causal SNP in the region and several enhancer elements targeting STXBP4 are located within the 53 kb association signal. Expression studies in breast tumor tissues found SNP rs2787486 to be associated with increased STXBP4 expression, suggesting this may be a target gene of this locus.

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)0.001
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.103
Threshold uncertainty score0.274

Codex and Gemma teacher scores by category

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

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 head0.015
GPT teacher head0.250
Teacher spread0.235 · 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.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
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

Citations24
Published2016
Admission routes2
Has abstractyes

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