Validated pipeline and the software for data analysis
AMP/ASCO/CAP and ACMG variants annotation
Time to result - 24 hours for 16 samples
GeneValue™ NSCLC Solution is designed to determinate significant genetic variants in non-small cell lung cancer (NSCLC) samples by NGS from human genomic DNA and total RNA isolated from Formalin-fixed, paraffin-embedded (FFPE).
Features
Specifications
Analyzed DNA regions
All coding regions (CDSs) of EGFR, KRAS, TP53,NRAS genes; 20-25 exons ALK; 11 и 15 exons BRAF; 16-21 exons ERBB2 (HER2); 2, 8, 10, 14, 21 exons PIK3CA; hotspots of MET and ROS1genes
Analyzed fusions
Any fusions for oncogenes: NTRK1, NTRK2, NTRK3, ALK, ROS1, RET Gene partner indication only for partners:AKAP13, IRF2BP2, SQSTM1, TRIM24, ETV6, TPM3, EML4, CD74, KIF5B
Exon skipping detection
MET exon 14 skipping; ERBB2 exon 16 skipping
Features
Specifications
Number of genes
23
Detected variants
DNA: SNV, INDEL RNA: exon skipping, fusions
Limitations
The kit is not intended for detection of CNV, extended STR and homopolymer variants
Analyte
DNA and RNA isolated from formalin-fixed, paraffin-embedded tissues (FFPE)