Optimize your targeted sequencing workflows
Targeted sequencing, which allows you to focus on sequences and region of interest, encapsulates two different techniques: a broad, target capture via a hybridization method or a PCR-based amplicon panel design. Among its most notable benefits of targeted sequencing compared to other methods in NGS such as whole genome sequencing, is the fact that because less genomic sequence is being interrogated, only target regions of interest are sequenced. This means that by focusing the sequencing real estate of the flow cell to only regions of interest, genomic sequences can be enriched anywhere from 100 to a 1 million times compared to DNA-sequencing.
Revvity offers an optimized workflow to meet your targeted sequencing needs.
For research use only. Not for use in diagnostic procedures.
Jumpstart your cancer research with a robust and powerful homogenizer designed to simplify sample preparation and prepare high quality lysates prior to nucleic acid extraction and targeted sequencing workflows.
Genomic DNA extraction
The isolation of high-quality genomic DNA from diverse sample materials is a crucial part of the genomic sequencing workflow. Learn more about Revvity´s solution for high performance DNA isolation workflows.
Genomic DNA and NGS library analysis
Improve your nucleic acid analysis with the LabChip® automated microfluidic capillary electrophoresis (micro-CE) technology and enable the analysis of genomic DNA and NGS libraries in seconds. Reporting is improved and simplified through the automatic generation of data as an electropherogram, virtual gel, or tabular report.
Whole exome and core exome library prep
Centred around the NEXTFLEX® Human Whole Exome Sequencing Panel and NEXTFLEX® Core Exome Sequencing v2 panel, Revvity’s standardized and tested targeted capture workflows ensure time and cost savings to labs that are looking to establish genetic analysis or expand their current test menu.
Increase on-target reads with blockers
During target enrichment, adapters can interact with the complementary adapter sequence strand of another library molecule. The NEXTFLEX® Universal Blockers are designed to prevent concatemerization of library molecules. By blocking this complementary adapter sequence interaction, the number of on-target reads improves dramatically and the depth of enrichment increases.
Automation of targeted sequencing workflows
Revvity NGS liquid handlers’ standardized deck configuration allows for complete liquid handling, thermal control, and waste management for complex application requirements in next generation sequencing sample preparation protocols. Revvity's liquid handler portfolio has validated protocols for several NGS applications, including whole genome sequencing, RNA seq, ChIPseq, targeted resequencing and amplicon sequencing.
Please note that product labeling (such as kit insert, product label, and kit box) may be different compared to the company branding. Please contact your local representative for further details.