eagle-i Oregon Health & Science UniversityOregon Health & Science University
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Copy number variation analysis

eagle-i ID


Resource Type

  1. Material analysis service


  1. Fee for service
  2. Resource Description
    "Whole Genome Genotyping Arrays: Human660W-Quad - More than 658,000 markers with an median spacing of 2.5 kb. Each slide assays four samples with as little as 200 ng of starting genomic DNA. Illumina HD arrays can achieve an average call rate of greater than 99%. The Human660W-Quad content is based on HapMap release 23. It offers high value coverage across many populations, captures the majority of known variation, and targets common CNV regions. It contains about 100,000 markers that specifically target regions of common copy number varation that were recurrently identified in a high-density CNV discovery project across mutiple population."
  3. Contact
    Harrington, Chris, Ph.D.
  4. Access Restriction(s)
    We accept samples from both the OHSU community and from non-OHSU academic and commercial institutions.
  5. Service Provided by
    Gene Profiling Shared Resource Core Laboratory
  6. Related Technique
    Solexa sequencing
Provenance Metadata About This Resource Record
Copyright © 2016 by the President and Fellows of Harvard College
The eagle-i Consortium is supported by NIH Grant #5U24RR029825-02 / Copyright 2016