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Deep Exome Sequencing Helps Researchers to Discover Causative Mutations

Illumina
26 Jun 2013

In this case study Dr Seth Crosby describes how the HiSeq® 2000 system and TruSeq® Exome Enrichment Kits are enabling GTAC studies and helping researchers discover mutations in cancer and constitutional disorders.

Links

IlluminaCompany website

Tags

DNA SequencingBiomarkersNext Generation SequencingCancer ResearchMutationSequencing

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