1. Imputation of KIR Types from SNP Variation Data
- Author
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Damjan, Vukcevic, James A, Traherne, Sigrid, Næss, Eva, Ellinghaus, Yoichiro, Kamatani, Alexander, Dilthey, Mark, Lathrop, Tom H, Karlsen, Andre, Franke, Miriam, Moffatt, William, Cookson, John, Trowsdale, Gil, McVean, Stephen, Sawcer, and Stephen, Leslie
- Subjects
Male ,DNA Copy Number Variations ,Genotype ,High-Throughput Nucleotide Sequencing ,hemic and immune systems ,chemical and pharmacologic phenomena ,Sequence Analysis, DNA ,Polymorphism, Single Nucleotide ,Asthma ,Article ,Dermatitis, Atopic ,Cohort Studies ,Europe ,Receptors, KIR ,Case-Control Studies ,otorhinolaryngologic diseases ,Humans ,Family ,Female ,Genetic Predisposition to Disease - Abstract
Large population studies of immune system genes are essential for characterizing their role in diseases, including autoimmune conditions. Of key interest are a group of genes encoding the killer cell immunoglobulin-like receptors (KIRs), which have known and hypothesized roles in autoimmune diseases, resistance to viruses, reproductive conditions, and cancer. These genes are highly polymorphic, which makes typing expensive and time consuming. Consequently, despite their importance, KIRs have been little studied in large cohorts. Statistical imputation methods developed for other complex loci (e.g., human leukocyte antigen [HLA]) on the basis of SNP data provide an inexpensive high-throughput alternative to direct laboratory typing of these loci and have enabled important findings and insights for many diseases. We present KIR∗IMP, a method for imputation of KIR copy number. We show that KIR∗IMP is highly accurate and thus allows the study of KIRs in large cohorts and enables detailed investigation of the role of KIRs in human disease.
- Published
- 2015