دورية أكاديمية
Additional file 1 of Rare copy-number variants as modulators of common disease susceptibility
| العنوان: | Additional file 1 of Rare copy-number variants as modulators of common disease susceptibility |
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| المؤلفون: | Chiara Auwerx, Maarja Jõeloo, Marie C. Sadler, Nicolò Tesio, Sven Ojavee, Charlie J. Clark, Reedik Mägi, Alexandre Reymond, Zoltán Kutalik |
| سنة النشر: | 2024 |
| مصطلحات موضوعية: | Genetics, Structural variation, CNV, GWAS, Time-to-event analysis, Common diseases, Pleiotropy, 16p13.11, 16p11.2, Genomic disorders |
| الوصف: | Additional file 1: Supplemental Notes. Note S1. Microarray-based CNV calling. Note S2. Sample filtering criteria. Note S3. Probe and covariate selection for main GWAS analysis. Note S4. Post-CNV-GWAS summary statistics processing. Note S5. Estonian Biobank replication. Note S6. Subgrouping of CNV carriers. Note S7. BRCA1 deletion association with ovarian and other female cancers. Note S8. LDLR deletion association with ischemic heart disease. Note S9. 16p12.2 deletion associations. Note S10. 22q11.2 CNV associations. |
| نوع الوثيقة: | article in journal/newspaper |
| اللغة: | unknown |
| العلاقة: | https://figshare.com/articles/journal_contribution/Additional_file_1_of_Rare_copy-number_variants_as_modulators_of_common_disease_susceptibility/24955993Test |
| DOI: | 10.6084/m9.figshare.24955993.v1 |
| الإتاحة: | https://doi.org/10.6084/m9.figshare.24955993.v1Test https://figshare.com/articles/journal_contribution/Additional_file_1_of_Rare_copy-number_variants_as_modulators_of_common_disease_susceptibility/24955993Test |
| حقوق: | CC BY + CC0 |
| رقم الانضمام: | edsbas.E3A17A02 |
| قاعدة البيانات: | BASE |
| DOI: | 10.6084/m9.figshare.24955993.v1 |
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