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Next-Generation Sequencing (NGS) is a powerful tool for answering your research questions, and it’s easier than you think. You don’t need to be an expert. Researchers can now partner with an accessible network of core labs for comprehensive NGS support. Illumina is here to help you! | Illumina, Inc.
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Using NGS to detect variation in the genome, epigenome and transcriptome is giving researchers more data to better understand cancer. Learn how multi-omics approaches are transforming personalized medicine research. Download the article: https://ilmnmkt.illumina.com/2016006358 | Illumina, Inc.
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