Human CGH Whole-Genome Exon-Focused Arrays
Human CGH Exon-Focused arrays provide complementary data to both exome and whole genome sequencing. These arrays enable genome-wide discovery of CNV's and they have enhanced capabilities of detecting small, exon-level copy number changes. The combination of exome/whole genome sequencing data and CGH data provide researchers with a more comprehensive data set to better explain disease.
Learn | Literature
- NEW! NimbleGen CGH 4.2M Platform Arrays
Sales Flyer (PDF Format 666KB) - 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
- 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.
