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ClearSeq Inherited Disease, XT
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Regulatory Status:
RUO
The ClearSeq Inherited Disease enables analysis of 2,742 genes known to cause inherited disorders.
- Publication Part Number: 5190-1505
- Created: 31 May 2011
- 142 KB
ClearSeq Inherited Disease Data Sheet
- Publication Part Number: 5991-4962EN
- Created: 16 July 2014
- 427 KB
| Chinese (Simplified) (China) | Complete (PDF) |
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Protocol for SureSelect XT HS2 RNA Library Preparation and Target Enrichment for the Illumina platform.
- Publication Part Number: G9989-90000
- Created: 16 May 2023
- 2 MB
Protocol for SureSelect XT HS2 RNA Library Preparation and Target Enrichment on the Agilent NGS Bravo Option A.
- Publication Part Number: G9993-90020
- Created: 15 Feb 2023
- 6 MB
Protocol for SureSelect XT HS2 RNA Library Preparation and Target Enrichment on the Agilent NGS Workstation Option B.
- Publication Part Number: G9993-90010
- Created: 11 Oct 2022
- 7 MB
Protocol for SureSelect XT HS2 DNA System, Automated using Agilent NGS Workstation Option B
- Publication Part Number: G9985-90010
- Created: 03 Oct 2022
- 5 MB
Protocol for SureSelect XT HS2 DNA System, Automated using Agilent NGS Bravo Option A
- Publication Part Number: G9985-90020
- Created: 03 Oct 2022
- 5 MB
SureSelect Target Enrichment System for Sequencing on Ion Proton Protocol
- Publication Part Number: G7530-90005
- Created: 23 Aug 2021
- 633 KB
SureSelect QXT Target Enrichment for Illumina Multiplexed Sequencing Protocol
- Publication Part Number: G9681-90000
- Created: 29 July 2021
- 800 KB
SureSelect XT Target Enrichment System for the Illumina Platform Protocol
- Publication Part Number: G7530-90000
- Created: 29 July 2021
- 1 MB