Accel-Amplicon® Plus Myeloid Panel

Deeply interrogate genes implicated in hematological malignancies.

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).

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 VarSome.
  • Compatible with all Illumina platforms.

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DATA SHEET
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PANEL-SPECIFIC BIOINFORMATICS FILES
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WORKFLOW
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PANEL SPECIFICATIONS
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PERFORMANCE DATA
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AVAILABLE DATA ANALYSIS
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PROTOCOLS, TOOLS & TECHNICAL NOTES
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