| Test Code |
Test Name |
Location |
Methodology |
Disease Category |
MRP |
Days |
|
MGM2499
|
DPU1085 : WHOLE GENOME SEQUENCING TEST - FOR GENETIC DISORDERS (TN SCHEME) |
Bangalore |
Next Generation Sequencing |
Rare inherited diseases |
167300 |
37 |
|
MGM275
|
Whole Genome Sequencing (Mean 30X) |
Bangalore |
Next Generation Sequencing |
Other |
167300 |
32 |
|
MGM1556
|
Tumour Mutation Burden (TMB) Analysis by NGS |
Bangalore |
Next Generation Sequencing |
Oncology |
52200 |
16 |
|
MGM1558
|
Comprehensive tumor panel (SNVs, InDels, CNVs & Fusions) + TMB (Tumor mutational burden) |
Bangalore |
Next Generation Sequencing |
Oncology |
52200 |
23 |
|
MGM1484
|
Prenatal sanger variant analysis [2 variants] |
Bangalore |
Sanger Sequencing |
Other |
20600 |
16 |
|
MGM2718
|
Oncotrack Advance -Liquid Biopsy NGS test (SNVs, InDels and Fusions) |
Bangalore |
Next Generation Sequencing |
Oncology |
82400 |
16 |
|
MGM1295
|
Additional family member (investigational) testing-3 variants |
Bangalore |
Sanger Sequencing |
Other |
18400 |
16 |
|
MGM1892
|
HRDTrack test |
Bangalore |
Next Generation Sequencing |
Oncology |
111500 |
23 |
|
MGM006
|
Fabry disease (GLA) gene analysis |
Bangalore |
Next Generation Sequencing |
Metabolic Disorders |
14000 |
21 |
|
MGM010
|
Achondroplasia (FGFR3) gene analysis |
Bangalore |
Next Generation Sequencing |
Skeletal dysplasia |
14000 |
21 |
|
MGM024
|
Sjogren-Larsson syndrome (ALDH3A2) gene analysis |
Bangalore |
Next Generation Sequencing |
Dermatology |
14000 |
21 |
|
MGM027
|
Androgen receptor (AR) gene analysis |
Bangalore |
Next Generation Sequencing |
Endocrinology |
14000 |
21 |
|
MGM038
|
Mondini defect (SLC26A4) gene analysis |
Bangalore |
Next Generation Sequencing |
ENT |
14000 |
21 |
|
MGM050
|
Factor VII deficiency (F7) gene analysis |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
|
MGM060
|
Von Willebrand disease (VWF) gene analysis |
Bangalore |
Next Generation Sequencing |
Hematology |
14000 |
21 |
|
|
|
|
