Illumina
HumanOmniExpress BeadChip Kits

Infinium FFPE DNA Restoration Solution

System: iScan, HiScanSQ
Technology: BeadArray
Assay: Infinium DNA Analysis Assay
Applications: Whole-Genome Genotyping and Copy Number Analysis
Species: Human

Archival formalin-fixed paraffin-embedded (FFPE) samples hold an abundance of invaluable information for human cancer studies. Because these samples generally yield highly degraded DNA, they perform poorly in most whole-genome genotyping studies. The Infinium HD FFPE DNA Restore Kit can repair these degraded DNA samples in preparation for use with the Infinium HD Assay. After DNA extraction using one of many commercially available kits, the Infinium HD FFPE QC Kit is used to evaluate the quality of prospective DNA samples to determine if they are usable. The kit provides primers for a real-time PCR assay that can be carried out using standard instrumentation available in most biological laboratories. Extracted FFPE samples that pass the QC test are then eligible for restoration using the Infinium HD  FFPE DNA Restore Kit.

Two 12-sample BeadChips, the HumanCytoSNP_FFPE-12 and HumanOmniExpress_FFPE, provide >250,000 and >600,000 genomic markers, respectively. The content on each array consists of intelligently selected tag SNPs that provide comprehensive coverage of the genome. With dense and even marker spacing, the BeadChip content can also be used to precisely detect structural aberrations, allowing researchers to accurately identify structural differences between paired-normal and tumor samples. The OmniExpress BeadChip provides coverage of 97% of the cancer genes identified by the Sanger Cancer Genome Project.

 

Order Information

WG-321-1001-PRE
Human
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Required Products

Product Workflow

A streamlined workflow to QC FFPE samples and restore viable DNA for whole-genome amplification using a modified protocol. The restored samples can be genotyped using the proven Infinium HD Assay. The assay results can be easily analyzed using highly intuitive, powerful DNA analysis tools in GenomeStudio Software.

FFPE DNA Restoration Solution Workflow


Applications

Whole-Genome Genotyping and Copy Number Variation Analysis

Genome-wide association studies (GWAS) map genetic variation across human populations to identify variants associated with human disease. Infinium HD BeadChips offer GWAS researchers the flexibility to profile samples with 300,000 to 1.2 million markers in high-throughput format, and deliver dense genome-wide coverage with the most up-to-date content available from the scientific community. Strategically selected probes provide sensitive copy number variation analysis and target high-value regions of the genome associated with disease.

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Cytogenetic Analysis

Structural variability is a substantial source of genetic varia­tion that has a major influence on phenotypic variation. Cytogenetic analysis allows researchers to profile chromosomal aberrations such as amplifications, deletions, rearrangements, point mutations, copy number changes, and copy-neutral loss of heterozygosity (LOH) events.

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GenomeStudio

Visualize and analyze data generated by all of Illumina's platforms using the GenomeStudio Data Analysis Software. This powerful informatics solution supports analysis of microarray-based data generated by the HiScanSQ System, iScan System, and BeadXpress Reader. Performance-optimized tools and a user-friendly graphical interface allow you to quickly and easily convert data into meaningful results.

Beeline

Beeline Software provides a direct path to project creation and sample management for large array experiments. The time required for data analysis is reduced by flexible allele-calling and data filtering prior to entry into GenomeStudio Data Analysis Software. Windows-based Beeline software works in conjunction with GenomeStudio software to support the analysis of data generated by Infinium and GoldenGate BeadChips.

iControlDB

Illumina's freely accessible iControlDB is an online database of genotype and phenotype data from individuals on all ILMN's GWAS arrays that can be used as controls for association or imputation studies.