Design Share Panels

Pre-designed NGS target enrichment panels
RUO For Research Use Only. Not for use in diagnostic procedures.

Customized panels backed by expert collaboration

Design Share panels are NGS target enrichment designs developed by Roche scientists and in collaboration with leading researchers around the world.

Featuring pre-designed content from research experts, Roche’s probe design expertise and performance data, the Design Share panels offer you the benefit of a confident and convenient entrance into the NGS Target Enrichment space. They are also fully customizable using the HyperDesign Tool, allowing you the flexibility to add or remove content to better suit your research needs.

There are panels currently available in: 

  • Somatic oncology research: KAPA HyperCap DS NHL Panel
  • Hereditary genetics and oncology research: KAPA HyperCap DS Inherited Disease Panel, KAPA HyperCap DS Sudden Cardiac Death Panel, KAPA HyperCap DS NeuroDegeneration Panel, KAPA HyperCap DS Hereditary Cancer Research Panel)
  • Metabolic disease research: KAPA HyperCap DS Human mtDNA Design.

If you would like to share your design on this page, please contact your local Roche sales representative. In case you are interested in fully verified and validated panels that are also off-the-shelf available, such as the KAPA HyperExome V2 Probes or the KAPA HyperCap Catalog Panels, please visit the respective pages.

Design share panels comparison overview

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Design share panels comparison overview

 

Research Area

Organism

Genome build

Specifications

Ordering information
Product type

Internal reference (IRN)

Material numbers and pack sizes

KAPA HyperCap DS NHL Panel

Somatic oncology research

Human

HG38

Covers 383 genes and regions commonly associated with B-cell lymphomas with a capture target size of 341 Kb. It can be used for longitudinal, robust, and sensitive detection of ctDNA in NHL research applications.

KAPA HyperChoice MAX 3Mb T1

1000028225

09052593001 for 24 rxn
09052615001 for 96 rxn

KAPA HyperCap DS Inherited Disease Panel

Hereditary genetics & oncology research

Human

HG38

Covers > 4100 genes and regions associated with inherited disease with a capture target size of 12.3 Mb.

KAPA HyperChoice Probes

1000004873

KAPA HyperChoice MAX 40Mb starting from 24 reaction packs:

09053352001 for 24 rxn
09053379001 for 48 rxn
09053387001 for 96 rxn
09053395001 for 192 rxn
09053409001 for 384 rxn

KAPA HyperCap DS Sudden Cardiac Death Panel

Hereditary genetics & oncology research

Human

HG38

Covers 152 genes and regions associated with cardiovascular conditions with a capture target size of 772 Kb.

KAPA HyperChoice Probes

1000004863

KAPA HyperChoice MAX 3Mb T3 starting from 12 reaction packs:

09052895001 for 12 rxn
09052909001 for 24 rxn
09052917001 for 48 rxn
09052925001 for 96 rxn
09052933001 for 192 rxn
09052941001 for 384 rxn

KAPA HyperCap DS NeuroDegeneration Panel

Hereditary genetics & oncology research

Human

HG38

Covers over 98 genes and regions associated with neurodegenerative disorders with a capture target size of 335 Kb.

KAPA HyperChoice Probes

1000004883

KAPA HyperChoice MAX 3Mb T1 starting from 12 reaction packs:

09052585001 for 12 rxn
09052593001 for 24 rxn
09052607001 for 48 rxn
09052615001 for 96 rxn
09052623001 for 192 rxn
09052631001 for 384 rxn

KAPA HyperCap DS Hereditary Cancer Research Panel*

Hereditary genetics & oncology research

Human

HG19

Covers 226 genes and regions commonly associated with hereditary cancer syndromes with a capture target size of 744 Kb.

KAPA HyperChoice Probes

1000007813

KAPA HyperChoice MAX 3Mb T3 starting from 12 reaction packs:

09052895001 for 12 rxn
09052909001 for 24 rxn
09052917001 for 48 rxn
09052925001 for 96 rxn
09052933001 for 192 rxn
09052941001 for 384 rxn

KAPA HyperCap DS Human mtDNA Design

Metabolic Disease Research

Human

HG38

Covers the Human mitochondrial genome with a primary target size of 16 Kb.

KAPA HyperChoice Probes

1000005603

KAPA HyperChoice MAX 0.5Mb T1 starting from 12 reaction packs:

09052143001 for 12 rxn
09052151001 for 24 rxn
09052160001 for 48 rxn
09052178001 for 96 rxn
09052186001 for 192 rxn
09052194001 for 384 rxn

Performance data is available. Please contact your local Roche office.
*Validation of CZECANCA (CZEch CAncer paNel for Clinical Application) for targeted NGS-based analysis of hereditary cancer syndromes. PLoS One. 2018 Apr 12;13(4):e0195761.

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HyperDesign Tool

The online, user-friendly HyperDesign Tool builds on two decades of in silico design experience to select probe panels that achieve deeper, more uniform downstream sequencing coverage with fewer sequencing reads—even across difficult-to-capture regions.

Contact us

Do you have questions about our products or services? We’re here to help. Contact a Roche representative in your region.

For Research Use Only. Not for use in diagnostic procedures.