The Accel-Amplicon Plus Myeloid Panel is a powerful tool for targeted gene sequencing. It combines content from peer reviewed publications and other sources to offer comprehensive and exon-level hotspot coverage of 23 clinically-relevant genes implicated in acute myeloid leukemia (AML), myelodysplastic syndrome (MDS) and myeloproliferative neoplasms (MPN).
And that’s just the beginning.
The panel is modular, allowing you to add on focused content to achieve your most optimal design. Either choose from our pre-validated content or add your own targets. We’ll work alongside you to design your assay and then Swift will optimize and wet-bench validate its performance before shipping it to you.
Now you have a more powerful tool to facilitate your project needs.
Comprehensive: Covers over 12,000 COSMIC and 1,900 ClinVar mutations and generates targeted libraries compatible with Illumina® sequencing platforms.
Informative: Provides full exon coverage of TP53 with flanking intron/exon boundaries.
Powerful: Simultaneous detection of single nucleotide variants (SNV) and small insertion and deletions (indels), all within a fast and easy single-tube assay workflow.
Flexible: Add your own targets using our pre-validated primers or others content. The possibilities are endless.
Other key features include:
Robust performance on cell-free DNA and FFPE samples starting with as little as 10 ng input.
Highly sensitive detection of rare variants down to 1% allele frequency.
Easy, single-tube assay with sequence ready libraries in 2 hours.
Streamlined analysis with bioinformatics resources such as Primerclip and Genialis.
Compatible with all Illumina platforms.