CGH Whole-Genome Tiling Arrays
NimbleGen CGH whole-genome tiling arrays offer comprehensive, unbiased, high resolution analysis if copy number changes across the genomes of multiple organisms.
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.
