Copy number variation analysis

eagle-i ID

Resource Type

Properties

1. Fee for service

   Yes

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