Solving the Cancer Puzzle with Next Generation Sequencing and Microarrays
21 May 2013

Cancer is a genetic disease that can be caused by many changes across the genome. This application article discusses how NGS is enabling an unprecedented understanding of the biology of cancer, providing opportunities for the accelerated development of diagnostics and novel therapeutic approaches that promise to revolutionize cancer care.

Illumina


Tags: epigenetics, cancer, miRNA, copy number variation, DNA methylation, NGS, exome sequencing, RNA-Seq, Genome Sequencing, genetic variation


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