Pioneer the path to precision genomics
With over 25 years of experience serving the cancer research community, we are focused on developing the right products, services, and support to meet the unique challenges of cancer genomics research.
With access to these innovative products and platforms, you can uncover the genetic variants and RNA signatures you need to power your next breakthrough.
Explore Oncomine assays and Ion AmpliSeq technology and panels.
Uncover RNA signatures that provide new insights in the identification, characterization, and progression of cancer subtypes.
Simple and fast library construction for affordable targeted sequencing.
Accurately screen or confirm somatic and germline variants of choice using sequencing and real-time PCR.
Focus your cancer research with end-to-end targeted sequencing solutions.
Identify epigenetic changes that occur during tumor progression.
Detect new biomarkers and develop future tests from NGS analyses of circulating tumor cells (CTCs) and cell-free DNA (cfDNA) in serially collected whole-blood research samples.
Discover new biomarkers for cancer research using exome sequencing.
Isolate pure populations of cancer cells from tumor tissues.
Microarrays are the platform of choice for detecting DNA structural variants (SV) such as chromosome insertions, duplications, and deletions.