Across the globe, laboratories are facing constant pressure to do more with less.
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KAPA HyperCap Workflow
Today’s healthcare hurdles can
hinder tomorrow’s outcomes
hinder tomorrow’s outcomes
As the possibility of truly personalized healthcare becomes a more immediate reality, translational researchers are being put into the spotlight. With optimized processes and automated workflows, researchers are able to spend less time sequencing and more time discovering.
Next-gen sequencing for the next-generation scientist
KAPA HyperCap Workflow marks a new chapter in the story of sequencing innovation.
With increased automation across Target Enrichment and Library Preparation workflows, researchers are free to focus on higher value-added tasks.
Facilitate rich, relevant, and influential research with:
- Reduced reliance on manual steps
- Faster and more predictable turnaround times
- Accurate and reliable results to meet market demand
"Decrease of duplicate rate, improvement
of on target bases rate and coverage uniformity,
deeper mean coverage with the same raw data."
KAPA HyperChoice Probes early access customer
Optimize precision, streamline sample prep
Do more with less
Process more samples with less effort using our advanced hybrid capture technology
More precise targeting
Target difficult genomic regions with a superior probe design algorithm
Develop your own designs
Create your ideal probe with the intuitive and user-friendly HyperDesign Tool
Improve workflows
Facilitate flexible and more efficient library construction for your research
Maximize your effort
Minimize hands-on and turnaround times with automated workflows
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
"Big improvement with single size selection." QUB Custom
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