Comprehensive sequencing solutions
Choose from gold-standard Sanger sequencing technology and fragment analysis on the capillary electrophoresis (CE) platform to flexible and scalable next-generation sequencing (NGS) to help your clinical research lab realize its full sequencing potential.
When we studied how labs large and small utilize sequencing in their research we found just one thing in common: they all do it differently. The reality is, it usually takes a wide range of solutions to discover, validate and produce actionable results.
Data analysis and data management are two areas that tend to get overlooked in the decision making process of which sequencing approach to choose.
As our knowledge of the genetics implicated in disease increases, the requirements to use a broad net to detect mutations in a limited sub set of genes reduces and gene panels will become the way forward as it will reduce the cost and data management burden.
Choose Sanger sequencing to:
- Study a small subset of genes linked to a defined phenotype
- Confirm NGS variants
- Detect minor allele fractions down to 5%
- Read contiguous sequences up to 1000 bases
Choose NGS to:
- Study diseases with higher levels of phenotypic heterogeneity
- Make unbiased queries of a large number of genes to discover novel variants
- Sequence up to 260 million reads per day
New to sequencing?
No matter which sequencing instrument you choose, we offer optimized reagents and consumables, intuitive analysis software, and world-class technical support.
New Capillary Electrophoresis Instruments Support Center
Find tips, troubleshooting help, and resources for support related to your capillary electrophoresis instruments.
New Next-Generation Sequencing Support Center
Find tips, troubleshooting help, and resources for your next-gen sequencing applications.
For Research Use Only. Not for use in diagnostic procedures.