Science

Discovery accesses a deep reservoir of specimens, facilities, technologies, and expertise to equip our researcher clients with large-scale, custom services in oncogene testing, sequencing, and ancillary genomic services.

  • Services developed and overseen by leading experts in the development and application of genomic and bioinformatic technologies and methods.
  • Vast clinical network and biorepository to source biospecimens for large-scale genomic characterization projects.
  • Sophisticated genomic laboratories designed specifically for high-throughput sequencing services to support translational and clinical-based projects.
  • Front-line genomic research tools including: RNAseq, CATCH-Seq, 10X Genomics' Chomium™ Platform, TruSight Tumor 170™.
  • Robust data management and project support, including delivery of raw sequencing data and bioinformatic analysis by highly skilled scientists with leading genomic analysis tools.

For more details about our genomic services, please begin a consultation with your business development manager or submit the form below.

Service

Discovery's genomic services identify relevant biomarkers in both cell and tissue samples, including blood, cell isolations, tissue dissociations, and FFPE. These services are designed to produce high-quality data. For example, our sequencing standards default to high-read depths unless lower read depths are specifically requested. 

The benefits of sourcing and genomically characterizing biospecimens from a single vendor partner include:

  • Reduced backlogs on internal laboratories and personnel
  • Biospecimens and lab services accessed from a single vendor
  • Dedicated point of contact across projects
  • Simplified logistics and contracting
  • Characterized samples relevant to your criteria
  • Expertise of respected professionals in genomic services

Oncogene Panels:

  • Microsatellite instability (MSI)
  • Specific mutational analysis -
    EGFR, BRAF, KRAS, HPV, NRAS, etc.
  • TruSight Tumor 170™

Sequencing:

  • Whole exome sequencing (WES)
  • Whole transcriptome analysis (RNAseq)
  • HLA sequencing via Complete MHC
  • Single-cell genomic analysis via 10x Genomics' Chromium™ platform

Ancillary Services:

  • DNA isolation and purification
  • RNA isolation and purification
  • Data management
  • Bioinformatic analysis

Connect With Us

Submit this form to start a conversation with Discovery to:

  • Discuss a genomics project
  • Ask any questions about our genomic services