CD Genomics provides a number of options for those looking to perform copy number variation (CNV) analysis on several different microarray platforms depending on the organism, starting material and size of your project.
Agilent aCGH Technology
Agilent's oligonucleotide aCGH platform offers genome-wide as well as customized profiling on 60-mer oligo CGH microarrays for human, mouse and rat. Agilent's CGH end-to-end solution consists of flexible microarray formats, optimized and easy-to-use protocol, high resolution microarray scanning and powerful analytics software.
Supports a variety of formats, probes, and species
Custom arrays with user-defined content
Commercial arrays with standard content
Both Affymetrix and Illumina offer solutions for CNV analysis using SNP arrays. CD Genomics provides wet lab and data analysis services for each platform.
Analyze SNP and CNV data across millions of markers
Estimate Log R ratio and B-allele frequency for copy number analysis
Call genotypes, normalize and cluster data, and generate SNP statistics
Export genotype data to various third party applications; access multiple CNV algorithms and CNV analysis tools
Generate a chromosomal heat map for examining copy number aberrations across the entire genome for multiple samples
Free advice on experimental design
Peace of mind of using a laboratory with extensive experience of running small, medium and large-scale projects
Excellent data quality