Introduce

Genetic variants screening for solid tumors

Lung

Gastric

Colon

Breast / Ovarian cancer

Melanoma, etc.

Working Process

Specification

SOLIDaccuTest™ DNA (CE-IVD) SOLIDaccuTest™ RNA
Technique NGS (Next generation Sequencing)
Compatible platforms Illumina / Miseq, MiSeqDx
Target enrichment Targeted sequencing / Hyb & capture method
Specimen FFPE tissues, biopsy
Quantity 8 runs (8-12 samples, up to 96 samples/pack)
Analysis solution NgeneAnalySys™
Target genes 84 genes 29 genes
Target size 270 kb 80 kb
Turn around time 3 days 3 ~ 3/5 days
Variants type SNV, CNV, INDEL Fusion, Alternative splicing,
Expression level

Performance

Composed of most target genes in targeted cancer therapy
Obtain high coverage uniformity across all targets
More efficient detection og cancer-causing mutations

variants detection rate in blind test ≥ 99% :
clinical samples tested

High reproducibility and increased depth og coverage

Information

Cat no. Products Quantity Storage

NGB131UWW

NGB131UWW-71
NGB131UWW-73
NGB131UWW-72
NGB131UWW-74

SOLIDaccuTest™ DNA (Approved CE-IVD)

  • DNA NGB Core-Library Prep Kit
  • NGB Core-Library Prep Index 1 Kit
  • NGB Core-Target Enrichment Kit
  • Target Enrichment Probe Kit
96rxn
(8runs)
-20 ℃

NGB132UWW

NGB132UWW-71
NGB132UWW-73
NGB132UWW-72
NGB132UWW-74

SOLIDaccuTest™ RNA

  • RNA NGB Core-Library Prep Kit
  • NGB Core-Library Prep Index 1 Kit
  • NGB Core-Target Enrichment Kit
  • Target Enrichment Probe Kit
96rxn
(8runs)
-20 ℃
NGB312UWW NGeneAnalySys™ 1.4 (Software for both germline and somatic analysis)