Translational research is growing increasingly complex:
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KAPA HyperCap Workflow
Put your laboratory’s reputation
and efficiency in your hands
and efficiency in your hands
Improving your team’s ability to work efficiently will help you better manage costs and more confidently stand behind the scientific value of their research.
Lead the way with our leading sample prep portfolio
Equip your team with the confidence of true cost effectiveness.
Streamlining operations will help to optimize daily processes to:
- Minimize hands-on time
- Shorten turnaround times
- Make the most of your time
"Seamless process to setup the workflow in our lab.
The hybridization washes are easier
and more streamlined than Supplier Z's."
KAPA HyperChoice Probes early access customer
Enhance mutation detection with improved cost efficiency
Superior probe design
Target difficult regions with an advanced algorithm
Design flexibility
Develop high-quality custom designs with the intuitive HyperDesign Tool
Uniform capture
Increase confidence with higher-fidelity hybrid capture probes
Value in numbers
Target difficult regions with an advanced algorithm
Single-vendor ordering
Starting from nucleic acid extraction, you can get everything you need in one place
With KAPA HyperCap Workflow you can reduce costs with efficiency at every step.
- Streamlined, targeted resequencing using custom and catalog panels
- Improved automation with less intervention
"Very satisfied with the results of the TE Early Access Program.
Duplication rate decreases, coverage uniformity improves a lot,
SSBC conversion rate (unique depth/overall depth) improves
a lot. With less sequencing raw data, they can get more
effective data to call variants. All the improvements lead to
a decrease of the sequencing cost and a higher confidence in variant
calling, especially for some originally poorly-covered regions."
KAPA HyperChoice Probes early access customer
Talk to your Roche representative to update your workflow!
See in detail how KAPA
HyperCap Workflow
can enrich your research
Enhance your sample prep process
from DNA input to enriched library,
ready to sequence