Mouse CGH Whole-Genome Tiling Arrays
Roche NimbleGen offers ultra-high resolution mouse CGH arrays in our 3x720K format for comprehensive analysis of DNA copy number variation. In addition to the 3x720K array format, we offer mouse 385K arrays in single slide, 4 slide sets and 8 slide sets.
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.
