Power to detect risk alleles using genome-wide tag SNP panels

• المؤلفون الرئيسيون: Eberle M.A., Ng P.C., Kuhn K., Zhou L., Peiffer D.A., Galver L., Viaud-Martinez K.A., Lawley C.T., Gunderson K.L., Shen R., Murray S.S.
• مؤلفون آخرون: MEDICINE
• التنسيق: مقال
• منشور في: 2019
• الموضوعات: article; controlled study; gene locus; gene mapping; gene sequence; genetic risk; genome analysis; genotype; high throughput screening; human; human genome; major histocompatibility complex; risk assessment; single nucleotide polymorphism; Alleles; Genome, Human; Haploidy; Humans; Polymorphism, Single Nucleotide; Risk Factors
• الوصول للمادة أونلاين: https://scholarbank.nus.edu.sg/handle/10635/161865
• المؤسسة: National University of Singapore

10.1371/journal.pgen.0030170