Archer LIQUIDPlex™ Universal Solid Tumor panel
Detect important alterations for multiple cancers with one ctDNA panel
Find single nucleotide variants, insertions, deletions, and copy number variations in ctDNA with targeted NGS of 29 genes relevant for NSCLC, breast, colorectal, melanoma, and other solid tumor cancer research.
Pinpoint low-frequency variants with LIQUIDPlex NGS panels for ctDNA.
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Learn how the LIQUIDPlex Universal Solid Tumor panel can identify key genomic alterations for your research.
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Panel specifications
| Specifications | |
|---|---|
| Targeted genes | 29 |
| Genomic alterations | SNVs, Indels, CNVs |
| Input cfDNA required | ≥5 ng |
| Recommended number of reads | 5 M |
| Hands-on time | <3.5 hours |
| Total library prep time | 1.5 days |
| Platform compatibility | Illumina® |
| Reagent format | Lyophilized |
| Supported sample types | Plasma |
Gene targets
Interested in adding a few genes to this panel?
Customize this NGS panel by adding any of our functionally-tested designs or create a new panel that fits your exact requirements with Assay Marketplace.
Benefits
- Detect confidently—A unique outlier detection algorithm leverages position-specific data to enable variant detection even at low allele frequencies, one of the many ways that Archer Analysis empowers you to detect confidently.
- Less QNS—Anchored Multiplex PCR (AMP™) chemistry is designed for compatibility with a wide range of sample types, including low-input samples such as cfDNA.
- Achieve efficiency—Parallel workflows across all Archer panels provides streamlined genomic characterization, while single use, reaction-sized lyophilized reagents minimize hands-on time and potential pipetting errors.
- Customize content—Work with our design experts to modify any panel to fit your lab's specific needs.
Ready to start?
Talk with our technical sales team. Learn how the LIQUIDPlex Universal Solid Tumor panel can identify key genomic alterations for your research.
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