Received on April 20, 2007
Accepted on September 11, 2007

Molecular Diagnostics and Genetics

Development of a Focused Oligonucleotide-Array Comparative Genomic Hybridization Chip for Clinical Diagnosis of Genomic Imbalance

¹ Children's Hospital Boston, Boston, MA, and Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA
² Children's Hospital Boston, Boston, MA, and Harvard Medical School, Boston, MA
³ Baylor College of Medicine, Houston, TX
⁴ Children's Hospital Boston, Boston, MA
⁵ Children's Hospital Boston, Boston, MA, and Harvard Medical School, Boston, MA, and Howard Hughes Medical Institute, Chevy Chase, MD
⁶ Center for Human Genetic Research, Massachusetts General Hospital, Boston, MA, and Harvard Medical School, Boston, MA

^* To whom correspondence should be addressed. E-mail: bai-lin.wu{at}childrens.harvard.edu.

Background: Submicroscopic genomic imbalance underlies well-defined microdeletion and microduplication syndromes and contributes to general developmental disorders such as mental retardation and autism. Array comparative genomic hybridization (CGH) complements routine cytogenetic methods such as karyotyping and fluorescence in situ hybridization (FISH) for the detection of genomic imbalance. Oligonucleotide arrays in particular offer advantages in ease of manufacturing, but standard arrays for single-nucleotide polymorphism genotyping or linkage analysis offer variable coverage in clinically relevant regions. We report the design and validation of a focused oligonucleotide-array CGH assay for clinical laboratory diagnosis of genomic imbalance.

Methods: We selected >10 000 60-mer oligonucleotide features from Agilent's eArray probe library to interrogate all subtelomeric and pericentromeric regions and 95 additional clinically relevant regions for a total of 179 loci. Sensitivity and specificity were measured for 105 patient samples, including 51 with known genomic-imbalance events, as detected by bacterial artificial chromosome–based array CGH, FISH, or multiplex ligation-dependent probe amplification.

Results: Focused array CGH detected all known regions of genomic imbalance in 51 validation samples with 100% concordance and an excellent signal-to-noise ratio. The mean SD among log₂ ratios of all noncontrol features without copy-number alteration was 0.062 (median, 0.055). Clinical testing of another 211 samples from individuals with developmental delay, unexplained mental retardation, dysmorphic features, or multiple congenital anomalies revealed genomic imbalance in 25 samples (11.9%).

Conclusions: This focused oligonucleotide-array CGH assay, a flexible, robust method for clinically diagnosing genetic disorders associated with genomic imbalance, offers appreciable advantages over currently available platforms.