| System: | iScan, BeadStation, BeadArray Reader, HiScanSQ |
|---|---|
| Technology: | BeadArray |
| Assay: | Infinium DNA Analysis Assay |
| Applications: | Cytogenetic Analysis, Whole-Genome Genotyping and Copy Number Analysis |
| Species: | Human |
| Contents: | Each kit contains 4-96 BeadChips, along with reagents for amplifying, fragmenting, hybridizing, labeling, and detecting 16-384 whole-genome genotyping samples |
The Human660W-Quad BeadChip offers comprehensive genomic coverage across many populations and the majority of known variation in regions of the genome, based on HapMap release 24 data. The broad, evenly spaced whole-genome marker set provides high genomic coverage for powerful genome-wide association studies. The entire panel of nearly 660,000 markers provides exceptional identification of known and novel structural variants.
The Human660W-Quad BeadChip was built on the HumanHap550 BeadChip. For powerful CNV and cytogenetic analysis, the dense backbone content is combined with an additional 100,000 markers that are highly informative for analyzing common CNV regions. These markers specifically target regions of common copy number variation that were recurrently identified in a high-density screen for CNVs that occur in two or more HapMap samples.
These BeadChips were developed in collaboration with researchers at The Centre for Applied Genomics, Hospital for Sick Children, Toronto, the Wellcome Trust Sanger Institute, and Harvard Medical School/Brigham and Women's Hospital.
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.
More...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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