Genetics

Wilson’s disease
TP53 Gene Mutations
UGT1A128 Variant Homozygosity
Tumour M2-PK
Tumour mutational burden (TMB)
MYC Gene Expression
Microsatellite Instability (MSI) or Mismatch Repair Deficiency (dMMR) (Deficient DNA Mismatch Repair)
KRAS Gene Mutation (Interferon Regulatory Factor)
Japanese Encephalitis Virus RNA - PCR - Qualitative
JAK2 (Janus Kinase 2) Gene Mutation
Interferon Regulatory Factor 4 (IRF4)
Foundation One CDx Genomic Test (F1CDx)
FLT3 (FMS-like tyrosine kinase 3)
chromosomes 3, 7, 17, and the 9p21
Chromosome 17p
ESR1 Gene Mutation
DPD Gene Mutation
Cystic Fibrosis F508 (CFTR F508)
D1 (CCND1)
BRCA1 & BRCA2 Gene Mutations
BRAF V600 Mutations
BCR ABL Fusion Gene (Philadelphia Chromosome)
BCL2 Gene Rearrangement
B-Cell Immunoglobulin Gene Rearrangement
ALK Rearrangement and Overexpression
70-Gene Signature (MammaPrint)
46-Gene Signature (Prolaris)
21-Gene Signature (Oncotype DX)
17-Gene Signature
5 Protein Signature (OVA1)
PCA3 mRNA
Programmed Death Ligand 1 (PD-L1)
RET Gene Fusions and Mutations
PML-RARA Gene Fusion
PIK3CA Gene
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