Human CGH Whole-Genome Tiling Arrays
Roche NimbleGen offers ultra-high resolution human CGH arrays with up to 4.2 million probes for comprehensive analysis of DNA copy number variation. In addition to the 4.2M array format, 3x1.4M, 3x720K and 12x135K multiplex arrays are available for higher throughput and cost-effective analysis of genome-wide copy number variation associated with a broad range of human diseases.
Learn | Literature
- NEW! NimbleGen CGH 4.2M & 3x1.4M Microarrays
Sales Flyer (PDF Format 1MB) - NimbleGen Human CGH Whole-Genome Arrays
Brochure (PDF Format 2.2MB) - Descriptions of HG18 and HG19 Annotation Files (Version 3.0)
Datasheet (PDF Format 409KB) - Human Genome HG19 Annotation Files
Annotation Files (ZIP Format 12.8MB)
What files are included in this download? - Human Genome HG18 Annotation Files
Annotation Files (ZIP Format 11.2MB)
What files are included in this download? - Array CGH using DNA from Formalin-Fixed Paraffin-Embedded (FFPE) Tissue Samples
Technical Note (PDF Format 2MB)
Learn | Webinars
- ASHG 2010
Identification of a Novel Locus Associated with the Common Birth Defect Spina Bifida
- ASHG 2010
Exonic aCGH for Copy Number Detection in Mitochondrial Diseases
Learn | Publications
- Jun 2010 | Blood
Telomere dysfunction and fusion during the progression of chronic lymphocytic leukaemia: evidence for a telomere crisis. - May 2010 | BMC Genomics
Copy number variation in the bovine genome. - Nov 2009 | Clin Cancer Res
Homozygous deletion of MTAP gene as a poor prognosticator in gastrointestinal stromal tumors. - Nov 2009 | Nat Genet
T (brachyury) gene duplication confers major susceptibility to familial chordoma.
