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Sequence Capture Service Service Available Now
Roche NimbleGen recently announced the launch of NimbleGen Sequence Capture Service. You can select genomic regions up to 5Mb for targeted enrichment from full complexity genomic DNA. Just send us genomic DNA — We return the enriched regions you selected. Suitable for high-throughput sequencing on instruments such as the 454 Genome Sequencer FLX system.Seize the Genome!
  • High Performance: Capture up to 5Mb total regions on a single array with high coverage and specificity.
  • Embedded Quality Controls: NimbleGen Sequence Capture arrays incorporate built-in control probes to ensure system performance.
  • Maximum Flexibility: Tailor the array design to capture your genomic regions or thousands of exons in parallel.
  • Substantial Savings: Save time and cost compared to PCR-based methods.

Free Workshop at ESHG 2008
Join us on Monday, June 2, 2008, in Barcelona, Spain, for a free Roche NimbleGen workshop during the ESHG 2008 Annual Meeting. This workshop will feature the latest applications of NimbleGen microarray technology in copy number variation, epigenetics, and targeted enrichment for high-throughput sequencing.

Register Now - Space is Limited for this Event!ESHG 2008
  • High-Throughput Detection of Exonic
    Copy-Number Changes Using NimbleGen Oligonucleotide-Based CGH-Array Technology

    Jamel Chelly, MD, PhD, Faculty of Medicine
    Institute Cochin, Hospital Cochin
  • High-Throughput Approaches for
    DNA Methylation Profiling

    Stephan Beck, PhD, Professor of Medical Genomics, UCL Cancer Institute,
    University College London
  • Sequence Capture for Medical Sequencing
    Daniel Turner, PhD, Head of Sequencing Technology Development,
    Wellcome Trust Sanger Institute


  •  See the Abstracts and Register