Custom SureSelect
Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s custom solutions allow you to target your regions of interest using our free web portal SureDesign. Custom solutions are available for DNA and RNA target enrichment.
Receive your quote directly from the manufacturer.
Essential for sequencing data for clinical studies
Sequencing for clinical studies
Psomagen helped us with the SureSelect Custom Panel for our warfarin study patient samples. The process was very easy and the results are consistent. The support staff is excellent as well and will answer all questions thoroughly.
Review Date: 16 Nov 2021 | Agilent Technologies
Agilent’s market leading SureSelect platform provides a complete portfolio of catalog and custom products, providing the flexibility you need from discovery to follow-up studies. Agilent’s custom solutions allow you to target your regions of interest using our free web portal SureDesign. Custom solutions are available for DNA and RNA target enrichment.
- Flexibility to capture from 1kb to 24Mb
- Easy design process using intuitive SureDesign software or Agilent’s Design Service
- Efficient workflows for post-capture (XT) and pre-capture (XT2) pooling
- Create SureSelect designs specific to your research needs using Agilent's SureDesign tool
- To download design .bed files, please visit SureDesign.
For Research Use Only. Not for use in diagnostic procedures.
How automation and integrated sample QC enhance a targeted long-read-sequencing workflow
Tuesday, November 4, at 16:00 GMT | 17:00 CET | 11:00 EST | 8:00 PST
As the demand for greater accuracy and efficiency in genetic analysis grows, new approaches are needed to overcome the blind spots of conventional sequencing methods. This webinar will showcase a fully automatable workflow that integrates Agilent SureSelect hybrid capture, Agilent automated electrophoresis systems for sample quality control with PacBio HiFi long-read sequencing.
In addition to discussing workflow, we’ll share case studies where long reads play a fundamental role in identifying genetic variants that may be missed by conventional sequencing in research studies.
Join us to learn how targeted long-read sequencing:
- Focuses on genes and regions of interest in genetic research, while reducing costs and boosting sequencing depth at key loci.
- Overcomes the limitations of short-read technologies, including challenges with pseudogenes, homologous loci, structural variants, complex transcript isoforms, splicing events, and difficult regions such as repetitive or GC-rich sequences.
- Enhances both analytical performance and laboratory efficiency through automation.
Key learning objectives:
- Gain practical insights into implementing an automated targeted long-read sequencing workflow in the laboratory.
- Identify the genetic mutation types best suited for targeted long-read sequencing approaches.
- Understand the analytical advantages of long-read sequencing compared with conventional short-read methods.
Who should attend?
Lab directors, molecular pathologists, research scientists, clinical lab technicians, and anyone running or interested in running NGS workflows.
Certificate of attendance
If you attend the live webinar, you will automatically receive a certificate of attendance, including a learning outcomes summary, for continuing education purposes.
If you view the on-demand webinar, you can request a certificate of attendance by emailing editor@selectscience.net.
For Research Use Only. Not for use in diagnostic procedures. PR7003-294
Agilent's SureSelect DNA kit to accelerate capture-based enrichment library preparation
The new kit promises enhanced performance and flexibility to power cancer and genetics research
