Array comparative genomic hybridization (CGH) is illuminating DNA copy number variations (CNV) throughout the genome to diagnose disease etiology and to help tailor treatment regimens for patients to ...

Comparative genomic hybridization (CGH) was developed to identify pathogenic DNA copy-number changes (e.g., duplications, deletions) on a genome-wide scale, and to map these changes to genomic ...

There is an increasing demand for comprehensive genome analyses of single cells. In cancer genetics, single-cell approaches allow monitoring minimal residual disease or the assessment of heterogeneity ...