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Human Genome CGH+SNP microarray

eagle-i ID

http://msm.eagle-i.net/i/0000012f-aacf-34f6-df00-15fb80000000

Resource Type

  1. Microarray

Properties

  1. Resource Description
    The Agilent SurePrint G3 Human Comparative Genomic Hybridization (CGH) platform has been extended to include a set of Single Nucleotide Polymorphism (SNP) probes on the same microarray. This allows for the simultaneous, high-resolution detection of copy number and copy-neutral variations, without running two separate microarray experiments. The same straight-forward Agilent CGH workflow is used to prepare the samples for hybridization to the SurePrint G3 Human CGH+SNP microarrays. Restriction digestion of genomic DNA allows genotyping of SNPs located in the enzymes’ recognition sites. After labeling and hybridization, CGH+SNP microarray data are analyzed using novel algorithms contained within Agilent’s Genomic Workbench software.
  2. Manufacturer
    Agilent Technologies
  3. Website(s)
    http://www.genomics.agilent.com/CollectionOverview.aspx?PageType=Application&SubPageType=ApplicationOverview&PageID=2394
  4. Related Technique
    Nucleic acid microarray assay
  5. Related Technique
    Copy number variation profiling
  6. Location
    Functional Genomics Core Laboratory
 
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Copyright © 2016 by the President and Fellows of Harvard College
The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016