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 ...
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 ...
The introduction of array comparative genome hybridization (CGH) into prenatal genetic diagnosis presents both challenges and controversy to the clinical cytogenetic community. The challenges are ...
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