Illumina Introduces the Infinium<sup>®</sup> HumanLinkage-12 Genotyping BeadChip

9 Sept 2007

Product news

Illumina, Inc. today announced the introduction of the Infinium HumanLinkage-12 Genotyping BeadChip, Illumina’s fifth multi-sample Infinium BeadChip and the Company’s first standard panel to take advantage of a twelve-sample format for linkage analysis.

The HumanLinkage-12 BeadChip offers the lowest cost per sample for linkage analysis plus industry-leading call rates, uniform marker distribution, and superior SNP content. Powered by the Infinium Assay, this linkage panel is available for $90/sample, a competitive price with a PCR-free protocol and easy workflow. This new addition to the Linkage portfolio complements Illumina’s GoldenGate® Human Linkage V Panel, which is particularly suitable for degraded samples such as formalin-fixed, paraffin-embedded (FFPE). The HumanLinkage-12 BeadChip is also available for researchers interested in conducting linkage analysis studies via Illumina’s FastTrack Genotyping Service.

Linkage analysis maps the location of disease-causing loci by identifying genetic markers that are co-inherited with the phenotype of interest. According to a paper published in the journal Human Molecular Genetics by the International Multiple Sclerosis Consortium significant additional power can be obtained using high-throughput SNP genotyping for linkage analysis. This study, which revisited previously typed complex disease family cohorts, also reported that higher success rates and accuracy were found with Illumina’s technology.

Building on the success of the GoldenGate panels, Illumina decided to deploy the same linkage content on the 12-sample Infinium BeadChip. “We continue to see a need for linkage analysis tools, and for a number of years have had great success with Illumina's GoldenGate Assay for these kinds of studies. Now, we plan to run between 40,000 and 50,000 samples using the Infinium Assay to study diseases spanning schizophrenia to obesity,” said Kimberly F. Doheny, Ph.D., Assistant Director of the Center for Inherited Disease Research (CIDR) and Director of the Genetics Resources Core Facility SNP Center of the Johns Hopkins Institute of Genetic Medicine.

Douglas F. Levinson, M.D, Professor of Psychiatry at Stanford University School of Medicine is a long-time user of Illumina's GoldenGate Human Linkage IV Panel and says, “We began using the GoldenGate Assay when we started a linkage scan of over 4,000 members of families with schizophrenia. This product provided us with increased robustness, and helped us achieve genotyping call rates of 99.9 percent and information content well over 90 percent, so no further fine-mapping was required.”

“The twelve-sample BeadChip and the flexibility of the Infinium Assay provide researchers with the industry’s most cost-effective method for studying linkage with the highest information content. As with any Infinium product, this panel can also be used to study copy number variation, which is gaining great momentum in medical genetic studies. Coupled with the industry’s best data quality, the HumanLinkage-12 BeadChip now makes it significantly easier for researchers to conduct studies that uncover links between familial genotypes,” said Carsten Rosenow, Ph.D., Senior Marketing Manager, DNA Analysis at Illumina.

Links

Tags

Genome AnalysisGenomics, the study of genomes, includes functional genomics, evolutionary genomics and comparative genomics. There are many genomic technologies such as DNA sequencing of whole genomes, computational biology and bioinformatics. DNA and nucleic acids must be isolated and concentrated from cells for analysis with kits, automated analyzers and software. Other useful technologies for studying genomics include PCR, microarrays and electrophoresis.Lab-on-a-ChipLab-on-a-chip (LOC) technology uses microfluidic chips, such as microarrays, to perform biochemical assays on a small scale. Benefits of lab-on-a-chip include the small volume of sample required as well as the speed of analysis. In selecting lab-on-a-chip devices consider the assay, cost, reliability, sensitivity and signal to noise ratio.Microarray AnalysisMicroarrays, also known as biochips, are used for the detection and analysis of multiple genes, proteins, antibodies, or biomarkers on a single microchip. This can reveal information on protein or gene expression, single nucleotide polymorphism (SNP), copy number variation (CNV), epigenetics and patient health in clinical diagnostic tests. Discover a range of microarray scanners and prefabricated antibody, protein, RNA and DNA microarrays for your analysis or consider creating your own custom microarrays with a microarray printer. Find the best microarray products in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.SNPs TechnologySingle nucleotide polymorphisms (SNPs) are individual base variations in a DNA sequence. SNPs are used in research to study predispositions to disease and drug discovery. Products for studying single nucleotide polymorphisms include SNP arrays and detection systems to detect polymorphisms, SNP typing systems for genotyping DNA, and PCR to amplify specific SNPs.DNA SequencingDNA sequencing, such as sanger sequencing, is a biological technique that determines the precise order of nucleotide bases in a fragment or template of DNA. DNA sequencers and genetic analyzers are based on capillary electrophoresis, where labeled DNA fragments are electrophoretically separated by size as they migrate through a polymer. Find the best DNA sequencing products, including DNA sequencing kits, genomic libraries and genetic identity kits in our peer-reviewed product directory: compare products, check customer reviews and receive pricing direct from manufacturers.
Illumina Introduces the Infinium<sup>®</sup> HumanLinkage-12 Genotyping BeadChip