The document describes Agilent's comprehensive portfolio of instruments, reagents, and microarrays for high-resolution, sensitive detection of genomic copy number changes and copy-neutral aberrations. It mentions the advantages of using a single microarray for simultaneous high-resolution detection of copy number changes and copy-neutral LOH, as well as the ability to easily customize array designs using eArray.
This document describes the Agilent SurePrint G3 CGH+SNP Microarray Platform, which supports cytogenetic studies by detecting genomic copy number changes and copy-neutral aberrations like loss of heterozygosity (LOH) and uniparental disomy (UPD) on a single array. The platform offers a comprehensive portfolio of instruments, reagents, and microarrays for high-resolution, sensitive detection.
| Median probe spacing | 7kb |
|---|---|
| Median probe spacing | 25kb |
| SNP selection | 65,000 SNPs |
| Input genomic DNA | 500 ng |
The platform detects copy number changes and copy-neutral changes like loss of heterozygosity (LOH) and uniparental disomy (UPD) on the same array.
No, the workflow conserves precious samples with only 500 ng of input genomic DNA and no amplification required.