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Array Comparative Genomic Hybridization Array CGH for Detection of Genomic Copy Number Variants
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High-resolution assessment of copy number variation

Alexander Dobrovic1

  • 1Translational Genomics and Epigenomics Laboratory, Olivia Newton-John Cancer Research Institute, Heidelberg, Victoria, Australia; School of Cancer Medicine, La Trobe University, Bundoora, Victoria, Australia; Department of Pathology, University of Melbourne, Parkville, Victoria, Australia. alex.dobrovic@onjcri.edu.au.

Clinical Chemistry
|April 5, 2015
PubMed
Summary

No abstract available in PubMed .

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Sequencing of the human genome has opened up several best-kept secrets of the genome. Scientists have identified thousands of genome variations that exist within a population. These variations can be a single nucleotide or a larger chromosomal variation.
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