Human Genome CGH Microarrays
RUO
Agilent Human CNV Microarrays provide high-resolution optimized probe design to enable genome-wide CNV identification and characterization. The dual color microarrays contain 60-mer high quality probes to provide the sensitivity and specificity required for CNV association studies.
For Research Use Only. Not for use in diagnostic procedures.
Product Details
Features
- Coding and non-coding human sequences represented
- Probes are annotated against NCBI Build 38 (UCSC GRCh38, Dec. 2013)
- Probe design and selection have been carefully optimized and validated for maximal sensitivity and specificity
- Agilent provides validated protocols and reagents to process fresh frozen (SureTag Labeling Kit) and FFPE samples (ULS Labeling Kit.)
- Multiple microarray formats available
Featured References
- Publications
-
- 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
.jpg)