The identification of structural chromosomal aberrations can provide insight into causative relationships with complex phenotypes - including intellectual disability, developmental delay, and congenital anomalies.
HumanCytoSNP-12 and CytoSNP-850k BeadChips are cytogenetic microarrays that leverage the investigative power of SNP genotypes to reliably detect chromosomal imbalances of copy number and allelic homozygosity, which are commonly associated with genetic constitutional disorders.
CytoSNP microarrays provide additional value to laboratories by being able to detect variations that may be missed by other technologies.
Traditional cytogenetic methods for the detection of only dosage anomalies (copy number imbalances) are unable to assess allelic homozygosity and therefore missing potentially significant findings. Including a high number of SNP markers into the cytogenetic testing method provides a comprehensive assessment of underlying chromosomal anomalies.
Illumina cytogenetic SNP microarrays offer a simple, reliable, unbiased method that demonstrates high resolution for assessing regions of copy number change and absence of heterozygosity.
Our industry-leading chromosomal microarrays target genes and regions of the genome that are highly associated with genetic disease to extract cytogenetic data that is significant to the investigator.
From library prep, arrays, and sequencing to informatics, Illumina next-generation solutions empower researchers and clinicians across the globe to find the answers they seek.
We’re here with all the resources you need to accelerate progress. In addition to onsite training, ongoing support, and phone consults, we offer webinars and courses around the world.
Illumina offers a cytogenetics product portfolio that provides insight into chromosomal aberrations and powerful analytical tools to enable quick assessment of the finding’s biological relevance.
A powerful, genome-wide scanning panel designed for efficient, high-throughput analysis of genetic structural variations.
Provides comprehensive coverage of relevant genes for studies associated with cancer and constitutional disorders.
Perform next-generation sequencing (NGS) and cytogenomic array scanning all on one system.