Custom CGH & CGH+SNP Microarrays
RUO
Agilent custom DNA microarrays are manufactured to order, using the same process as our catalog products. Our patented SurePrint technology generates oligonucleotides with high complexity and sequence fidelity. A simple web interface, Suredesign, can be used to intuitively design, upload or search probes and include them in a final design.
Our human probe database contains over 28 million predesigned, in silico-validated human CGH and SNP probes. The probes span exonic, intronic, intergenic, CNV, pseudoautosomal, and segmented duplication DNA regions. Probes are optimized for enhanced sensitivity, enabling streamlined creation of CGH and CGH+SNP microarrays.
Our human probe database contains over 28 million predesigned, in silico-validated human CGH and SNP probes. The probes span exonic, intronic, intergenic, CNV, pseudoautosomal, and segmented duplication DNA regions. Probes are optimized for enhanced sensitivity, enabling streamlined creation of CGH and CGH+SNP microarrays.
For Research Use Only. Not for use in diagnostic procedures.
Product Details
Features
- Custom arrays are available in a variety of formats, allowing to run from 1 to 24 independent samples per slide based on desired thoughput.
- Custom arrays can be provided in both HD and G3 format, the two formats have different feature size: HD 60um, G3 30um.
- SureDesign provides the ability to create fully customized content uploading your own pre-designed probes or choose from predefined content.
- There is no minimum order requirement. Order just one and scale up based on your research needs, limiting validation costs.
- Creation of human CGH and CGH+SNP is streamlined thanks to the acess to a database of more than 28 million predesigned, in silico-validated human CGH probes.
- Available SureDesign probes span exonic, intronic, intergenic, CNV, pseudoautosomal, and segmented duplication DNA regions. The system also contains human SNP probes for ~100,000 SNPs.
- Probe design and selection have been carefully optimized and validated for maximum sensitivity and specificity.
- SureDesign allows you to create custom arrays for human, rat and mouse samples. For other species please contact our tech support.
- All reagents are manufactured in an ISO 13485 certified facility for ensured compliance
Applications
Featured References
- Publications
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- Pinto D et al. Comprehensive assessment of array-based platforms and calling algorithms for detection of copy number variants. Nat Biotechnol. 2011 May 8;29(6):512-20. doi: 10.1038/nbt.1852 [Application: General] Learn More
- Alesi V et al. Easychip 8x15k: A New Tool for Detecting Chromosome Anomalies in Low Risk Pregnancies, Supporting and Integrating Standard Karyotype J Genet Syndr Gene Ther 7: 277. doi:10.4172/2157-7412.1000277 [Application: Prenatal] Learn More
- Chau MHK et al. Characteristics and mode of inheritance of pathogenic copy number variants in prenatal diagnosis. Am J Obstet Gynecol. 2019 Nov;221(5):493.e1-493.e11. doi: 10.1016/j.ajog.2019.06.007. Epub 2019 Jun 14. [Application: Prenatal] Learn More
- Ribeiro et al. Upper aerodigestive tract carcinoma: Development of a (epi)genomic predictive model for recurrence and metastasis. Oncol Lett. 2020 May;19(5):3459-3468. doi: 10.3892/ol.2020.11459. Epub 2020 Mar 12 [Application: Cancer] Learn More
- Kaur et al. Clinical impact of chromothriptic complex chromosomal rearrangements in newly diagnosed multiple myeloma. Leuk Res. 2019 Jan;76:58-64. doi: 10.1016/j.leukres.2018.12.005 [Application: Cancer] Learn More
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