Custom CGH Arrays
The inherent flexibility of 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. Custom designs can be created with uniform or mixed-density probe spacing using the most current genome sequence from any eukaryotic genome.
Learn | Literature
- NimbleGen Copy Number Variation (CNV) Arrays
Datasheet (PDF Format 1.4MB) - 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? - Detecting Copy Number Variants Associated with Basal Cell Carcinoma in an Arsenic-Exposed Population
Application Note (PDF Format 1.2MB) - High Resolution Copy Number Analysis of Parkinson’s Samples Using Nexus Copy Number and Roche NimbleGen Microarrays
Whitepaper (PDF Format 964KB)
Learn | Webinars
- 30 Jun 2011
Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy
Learn | Publications
- Sep 2011 | Cell
Chromosome catastrophes involve replication mechanisms generating complex genomic rearrangements. - Jun 2011 | Neuron
Rare de novo and transmitted copy-number variation in autistic spectrum disorders. - May 2011 | Appl Environ Microbiol
Comparative genomics of Escherichia coli strains causing urinary tract infections. - April 2011 | Fertil Steril
Complex X chromosome rearrangement delineated by array comparative genome hybridization in a woman with premature ovarian insufficiency.
