Illumina Mouse LD Linkage

Mouse LD Linkage

System: iScan, iScanSQ, BeadArray Reader
Technology: BeadArray
Assay: GoldenGate Genotyping Assay
Applications: Linkage Analysis
Species: Mouse
Contents: Single OPA tube containing an optimized set of 377 loci

The mouse has been increasingly recognized as an optimal animal for the study of the genetics of complex disease traits. Two Mouse Linkage Panels (Mouse Low Density [LD] Linkage and Mouse Medium Density [MD] Linkage) are available for mouse genetics applications. These single nucleotide polymorphism (SNP) panels offer a low-cost, efficient, method for attaining genome-wide genetic data to identify quantitative trait loci (QTL), map candidate genes, and increase genotyping throughput.

With the completion of the mouse genome project, greater than 13,000 SNPs have been genotyped across 480 mouse strains using the Illumina GoldenGate Genotyping Assay. This SNP set is available from the Wellcome-CTC Mouse Strain SNP Genotype Set.

The Mouse LD Linkage Panel consists of 377 loci and has been optimized for application to N2 and F2 mouse genetics crosses, those typically used for mapping QTLs. This panel provides approximately 175-200 informative markers per cross and covers the entire mouse genome.

The Mouse LD Linkage Panel was designed to include approximately four SNPs per 27 Mb interval. At least one SNP in each interval was chosen to be informative in crosses involving the C57Bl/6J strain. On average, at least one SNP in each interval is informative for 85% of all possible strain combinations.

Specifications

Learn more about how this product is used. 


Mouse LD Linkage

Applications

Linkage Analysis

Linkage analysis provides researchers a powerful method for mapping the location of disease-causing loci by identifying genetic markers that are co-inherited with a phenotype of interest.  Illumina's linkage analysis BeadChips present the optimal solution for identifying regions of statistically unequivocal linkage by delivering the information content, call rates, and accuracy that enable discovery of links between familial genotype and phenotype in both monogenic and polygenic disorders.

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Order Information

GT-18-121
Mouse
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