Sentosa SQ Leukemia Panel

Detect sequence variants in leukemia samples


The Sentosa SQ Leukemia Panel is a DNA-based Next Generation Sequencing (NGS) assay that identifies gene mutations including single-nucleotide variants (SNVs) and insertions and deletions (indels) on a single platform. The panel is designed to detect approximately 3,312 mutations in 49 key cancer genes.  The genes selected for this panel include targets associated with acute myeloid leukemia (AML), myelodysplastic syndrome (MDS), and myeloproliferative neoplasms (MPN) as well as ALL, CML, and CLL.

The highly automated Sentosa SQ NGS workflow with Sentosa SQ Leukemia Panel begins from the extraction of peripheral blood samples, to the generation of reports within 2.5 days .  This workflow requires less than 3.5 hours of hands-on time. 


For more information on the genes and target mutations, please contact authorized Vela Diagnostics representatives.


Supporting Decision-Making:

  • Automated and user-friendly results interpretation with Sentosa SQ Reporter
  • Panel includes targets associated with AML, MDS, MPN, ALL, CML and CLL

Providing Laboratory Efficiency:

  • From sample to result in 2.5 days
  • Minimal input of 250 μl peripheral blood per library



Sample Input Peripheral Blood Samples
Target Genes 49
Target Amplicons 287
Target Mutations 3,312
Hands-on Time ≤ 3.5 hours
Turn-around Time ≤ 2.5 days


Sentosa SQ Leukemia Panel RUO EN



ProductPack SizeItem Number
Sentosa SQ 318 Chip Kit (8) RUO 8 runs 300301
Sentosa SQ Leukemia Reagents (4x8) RUO 4x8 300374
Sentosa SQ Leukemia Solutions (4x8) RUO 4x8 300372
Sentosa SQ Sequencing Reagents (8) RUO 8 300310
Sentosa SQ Sequencing Solutions (8) RUO 8 300314
Sentosa SQ Sequencing Supplies (8) RUO 8 300304
Sentosa ST Template Beads (8) RUO 8 300320
Sentosa ST Template Reagents (8) RUO 8 300317
Sentosa ST Template Solutions (8) RUO 8 300323
Sentosa ST Template Supplies (8) RUO 8 300326
Sentosa SX Whole Blood Kit (4x8) RUO 4x8 300251