Cow Genome Research
CGH/CNV
For comprehensive, unbiased analysis of DNA copy number changes we offer Cow CGH 385K Whole-Genome Tiling Arrays. For your custom research needs Roche NimbleGen’s array technology enables the rapid prototyping of custom array designs, which can include whole genomes, single chromosomal regions, or multiple loci of interest.
Learn | Literature
- NimbleGen Arrays User's Guide: CGH and CNV Arrays (Version 8.1)
User's Guide (PDF Format 2.6MB) - Array CGH using DNA from Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Samples
Technical Note (PDF Format 2MB) - Detecting Copy Number Variants Associated with Basal Cell Carcinoma in an Arsenic-Exposed Population
Application Note (PDF Format 1.2MB)
Learn | Webinars
Dr. Scott Selleck
Copy Number Variation in Low Copy Repeat-Rich Regions of the Genome: How Much is There and What Does it Take to Measure It?
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View Flash MovieDr. Heather Mefford
Genome Architecture and Genomic Disease: A Targeted Approach to Disease DiscoveryDownload MP3Download Video PodcastView Flash Movie
Learn | Publications
- May 2010 | BMC Genomics
Copy number variation in the bovine genome. - Oct 2006 | Physiol Genomics
Identification of estrogen-responsive genes in the parenchyma and fat pad of the bovine mammary gland by microarray analysis. - Sep 2006 | BMC Genomics
Butyrate induces profound changes in gene expression related to multiple signal pathways in bovine kidney epithelial cells.
