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  • Sequencing 500 genomes

    HiSeq will be used to generate sequence data for the 500 genomes.

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  • Enabling high-throughput counting applications

    Exponential growth in the number of reads per run are empowering new studies.

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  • Advancements in the study of cancer genomics

    Researchers are making new insights into cancer progression, diagnosis, and treatment.

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  • Tumor Heterogeneity Findings Impact Personalized Medicine Approaches

    Data generated on the HiSeq 2000 systems help identify intratumor heterogeneity.

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See how researchers are using NGS to solve problems:

Cancer
Cancer Microbiology
Microbiology Agriculture
Agriculture Forensics
Forensics Genetic Disease
Genetic Disease

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