CDAmp™ Myeloid Neoplasms Panel for comprehensive mutation profiling of myeloid malignancies via multiplex PCR-based targeted resequencing utilizing proprietary CDAmp technology. It includes the coding sequence (CDS) regions of 18 genes and hotspot mutation regions of 40 genes. It is designed for disease investigation and classification, molecular feature correlation analysis, therapeutic guidance research, and genetic screening of myeloid neoplasms such as acute myeloid leukemia (AML), myelodysplastic syndromes (MDS), myeloproliferative neoplasms (MPN), and MDS/MPN overlap syndromes.
Comprehensive Mutation Profiling
· Detects somatic mutations in 18 genes with full CDS coverage and 40 genes with targeted hotspot regions, including SNVs, indels, and internal tandem duplications (e.g., FLT3).
Fast, Simplified Workflow
· Prepare sequencing-ready libraries in a single tube within 5 hours, with less than 2 hours of hands-on time.
Superb Coverage Uniformity
· Ensures high uniformity of coverage even in high-GC regions for reliable variant calling.
| Enrichment Method: | Multiplex PCR Amplification |
| Species: | Human |
| Variant Types: | SNV、Indel、ITD |
| Target Size: | 6.5 Kb |
| Primer Count: | 766 |
| Amplicon Length: | 215bp(169-260bp) |
| Cancer Type: | AML、MDS、MPN、MDS/MPN |
| Number of Genes: | 58 |
| Sample Type: | blood,Bone Marrow etc. |
| Input DNA/RNA: | 10-80ng |
| Method: | NGS |
| Sequencing Platform: | Illumina; Ion Torrent |
| Storage: | Store at -20 °C. |
| ABL1 | ANKRD26 | ASXL1 | ATRX | BCOR | BCORL1 | BRAF |
| CALR | CBL | CBLB | CBLC | CDKN2A | CEBPA | CSF3R |
| CUX1 | DDX41 | DNMT3A | ETNK1 | ETV6 | EZH2 | FLT3 |
| GATA1 | GATA2 | GNAS | HRAS | IDH1 | IDH2 | IKZF1 |
| JAK2 | JAK3 | KDM6A | KIT | KMT2A | KRAS | MPL |
| NF1 | NPM1 | NRAS | PDGFRA | PHF6 | PIGA | PPM1D |
| PTEN | PTPN11 | RAD21 | RUNX1 | SETBP1 | SF3B1 | SMC1A |
| SMC3 | SRSF2 | STAG1 | STAG2 | TET2 | TP53 | U2AF1 |
| WT1 | ZRSR2 |
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