Enhancing linkage analysis of complex disorders: an evaluation of high-density genotyping.
To explore the potential value of recently developed high-density linkage mapping methods in the analysis of complex disease we have regenotyped five nuclear families first studied in the 1996 UK multiple sclerosis linkage genome screen, using Applied Biosystems high-density microsatellite linkage mapping set, the Illumina BeadArray linkage mapping panel (version 3) and the Affymetrix GeneChip Human Mapping 10K array. We found that genotyping success, information extraction and genotyping accuracy were improved with all systems. These improvements were particularly marked with the SNP-based methods (Illumina and Affymetrix), with little difference between these. The extent of additional information extracted is considerable, indicating that reanalysis of existing multiplex families using these newer systems would substantially increase power.
Duke Scholars
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- United Kingdom
- Polymorphism, Single Nucleotide
- Multiple Sclerosis
- Microsatellite Repeats
- Humans
- Genotype
- Genetics & Heredity
- Genetic Markers
- Evaluation Studies as Topic
- Chromosome Mapping
Citation
Published In
DOI
ISSN
Publication Date
Volume
Issue
Start / End Page
Location
Related Subject Headings
- United Kingdom
- Polymorphism, Single Nucleotide
- Multiple Sclerosis
- Microsatellite Repeats
- Humans
- Genotype
- Genetics & Heredity
- Genetic Markers
- Evaluation Studies as Topic
- Chromosome Mapping