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S.No Test_Code Test Type Method Description Sample Schedule TAT
S.No Test_Code Test Type Method Description Sample Schedule TAT
1 BGSNG72 SANGERS SEQUENCING MLPA + Sanger's MGMT METHYLATION BY MLPA + SANGERS FFPE TISSUE BLOCK DAILY 10
2 BGSNG71 SANGERS SEQUENCING SANGERS PATERNITY TESTING - 2 PARENTS & 1 CHILD STR ANALYSIS by IDENTIFILER WB in EDTA DAILY 7 DAYS
3 BGSNG70 SANGERS SEQUENCING SANGERS PATERNITY TESTNG - 1 PARENT & CHILD WB in EDTA DAILY 7 DAYS
4 BGSNG68 SANGERS SEQUENCING Sangers Hepatitis C Virus (HCV) – Genotyping WB in EDTA DAILY 3 DAYS
5 BGSNG67 SANGERS SEQUENCING Sangers Hepatitis B Virus (HBV) Drug Resistance Assay WB in EDTA DAILY 3 DAYS
6 BGSNG66 SANGERS SEQUENCING Sangers Hepatitis B Virus (HBV) – Genotyping WB in EDTA DAILY 3 DAYS
7 BGSNG65 SANGERS SEQUENCING Sangers AML - NPM1 ( Nucleophosmin -1) gene mutation Assay WB in EDTA DAILY 7 DAYS
8 BGSNG64 SANGERS SEQUENCING Sangers AML - FLT3 (fms like tyrosine kinase 3) Gene Mutation Assay WB in EDTA DAILY 7 DAYS
9 BGSNG63 SANGERS SEQUENCING Sangers AML - CEBPA (CCAAT/Enhancer Binding Protein) mutations WB in EDTA DAILY 7 DAYS
10 BGSNG62 SANGERS SEQUENCING Sangers AML PCR PANEL II - FLT3, NPM1 & C/EBPA ( With Normal Cytogenetics) WB in EDTA DAILY 7 DAYS
11 BGSNG61 SANGERS SEQUENCING Sangers KRAS, NRAS, BRAF MUTATION ANALYSIS WB in EDTA DAILY 7 DAYS
12 BGSNG60 SANGERS SEQUENCING Sangers Thiopurine Methyltransferase (TPMT - *2, *3A, *3B, *3C) Genotyping Peripheral blood DAILY 7 days
13 BGSNG59 SANGERS SEQUENCING Targeted mutation Analysis (more than 2 mutations) Peripheral blood/Amniotic fluid / Cord Blood/Chorionic villi - 10-15 days
14 BGSNG58 SANGERS SEQUENCING Targeted mutation Analysis (2 mutations) Peripheral blood/Amniotic fluid / Cord Blood/Chorionic villi - 10-15 days
15 BGSNG57 SANGERS SEQUENCING Targeted mutation Analysis (1 mutation) Peripheral blood/Amniotic fluid / Cord Blood/Chorionic villi - 10-15 days
16 BGSNG56 SANGERS SEQUENCING Solid tumor Combo1 [EGFR,ALK1,ROS1,MET,PD L1] Tumor tissue - 5-7 days
17 BGSNG55 SANGERS SEQUENCING SANGER SEQUENCING QF PCR Panel [13,18,21,XY] + MCC Amniotic fluid / Chorionic villi/ Cord Blood - 7 days
18 BGSNG54 SANGERS SEQUENCING Pre-implantation Genetic Disorder/PGD HLA Typing (Single Embryo) Trophectoderm - 15-20 days
19 BGSNG53 SANGERS SEQUENCING Pre-implantation Genetic Disorder/PGD (Single Embryo) with maternal DNA contamination check Trophectoderm + EDTA blood of mother for MCC - 15-20 days
20 BGSNG52 SANGERS SEQUENCING Pre-implantation Genetic Disorder/PGD (Single Embryo- 1 mutation) Trophectoderm - 15-20 days
21 BGSNG51 SANGERS SEQUENCING Pre-implantation Genetic Disorder/PGD (Single gene Disorder- Known mutation)- Baseline Peripheral blood of parents and affected child - 15-20 days
22 BGSNG50 SANGERS SEQUENCING SANGERS SEQUENCING POLE gene Mutation Analysis FFPE - 7-8 days
23 BGSNG49 SANGERS SEQUENCING PIK3CA Mutation Analysis (Exon 7, 9 & 20) Tumor tissue - 7-8 days
24 BGSNG48 SANGERS SEQUENCING NRAS Mutation Analysis (codons 12 & 13) Tumor tissue - 7-8 days
25 BGSNG47 SANGERS SEQUENCING NPM1 Mutation Analysis (Exon 12 insertion) Bone Marrow/Peripheral Blood - 7-8 days
26 BGSNG46 SANGERS SEQUENCING SANGERS NUDT15 gene Mutation analysis Peripheral Blood DAILY 7-8 days
27 BGSNG45 SANGERS SEQUENCING Myeloproliferative Leukemia Mutation Screening (MPL - S505N; W515L) Bone marrow / Peripheral blood - 7-8 days
28 BGSNG44 SANGERS SEQUENCING MYD88 gene Mutation Peripheral blood/Tumor tissue - 5-7 days
29 BGSNG43 SANGERS SEQUENCING Microsatellite Instability (MSI) (Lynch Syndrome/Colorectal Cancer) Peripheral blood - 7-8 days
30 BGSNG42 SANGERS SEQUENCING MECP2 Full Gene Mutation Analysis (RETT Syndrome) Peripheral blood - 8-10 days
31 BGSNG41 SANGERS SEQUENCING KRAS Mutation Screening (Codons 12 & 13) Tumor tissue - 7-8 days
32 BGSNG40 SANGERS SEQUENCING Jak 2 Mutation Detection Panel (Exons 12) Bone Marrow/Peripheral Blood - 7-8 days
33 BGSNG39 SANGERS SEQUENCING Jak2 Mutation Detection Panel (Exons 12-15) Bone marrow / Peripheral blood - 7-8 days
34 BGSNG38 SANGERS SEQUENCING Irnotecan Toxicity Assessment Peripheral Blood - 7-8 days
35 BGSNG37 SANGERS SEQUENCING IGHV Mutation load Bone marrow / Peripheral blood - 7-8 days
36 BGSNG36 SANGERS SEQUENCING IDH1 & IDH2 Mutation Analysis Tumor tissue - 7-8 days
37 BGSNG35 SANGERS SEQUENCING Human Papilloma Virus - HPV16, 18 & HIGH RISK GENEOTYPES Cervical swab - 7-8 days
38 BGSNG34 SANGERS SEQUENCING Human Inmmuno-defecincy Virus - 1 (HIV-1) Drug Resistance Genotype Peripheral blood/Plasma/Serum - 20-21 days
39 BGSNG33 SANGERS SEQUENCING HLA-B*57:01 Genotyping (for Abacavir Hypersensitivity) Peripheral blood - 7-8 days
40 BGSNG32 SANGERS SEQUENCING HLA-DRB1*1501 Genotyping (Multiple Sclerosis) Peripheral blood - 7-8 days
41 BGSNG31 SANGERS SEQUENCING HLA-B*1502 Genotyping (Carbamazepine) Peripheral blood - 7-10 days
42 BGSNG30 SANGERS SEQUENCING Hepatitis C Virus (HCV) Genotype Peripheral blood/Plasma - 20-21 days
43 BGSNG29 SANGERS SEQUENCING Hepatitis B Virus (HBV) Genotype Peripheral blood/Plasma - 7-8 days
44 BGSNG28 SANGERS SEQUENCING Hemochromatosis HFE Full Peripheral blood - 4-6 weeks
45 BGSNG27 SANGERS SEQUENCING Hemochromatosis Common Mutation Analysis in HFE Gene (H63D, S61C & C282Y) Peripheral blood - 7-10 days
46 BGSNG26 SANGERS SEQUENCING GATA2 Full length gene sequencing (Chronic Neutropenia, MonoMac Syndrome, Mylodysplasia, AML) Bone Marrow/Peripheral Blood - 15 days
47 BGSNG25 SANGERS SEQUENCING GATA1 Full length gene sequencing Bone Marrow/Peripheral Blood - 15 days
48 BGSNG24 SANGERS SEQUENCING 5-Flurouracil (5-FU) Toxicity and Chemotherapeutic Response (DPYD variants) Peripheral blood - 3-4 days
49 BGSNG23 SANGERS SEQUENCING Erythropoetin receptor gene Mutation Analysis Peripheral blood - 7-8 days
50 BGSNG22 SANGERS SEQUENCING Sanger's Sequencing Fragile X (FMR1) Carrier Screening Peripheral blood DAILY 12 days
51 BGSNG21 SANGERS SEQUENCING Epidermal Growth Factor Receptor Mutation Analysis (EGFR - Exon 18, 19, 20, 21) Tumor tissue - 3-4 days
52 BGSNG20 SANGERS SEQUENCING DMD carrier screening (79 Exons) Peripheral blood - 7-10 days
53 BGSNG19 SANGERS SEQUENCING CXCR4 gene Mutation Peripheral Blood - 7-8 days
54 BGSNG18 SANGERS SEQUENCING Cytochrome P450 2C19 Genotyping (CYP2C19) Clopidogrel resistance (*2,*3,*4,*10) Peripheral blood - 7-8 days
55 BGSNG17 SANGERS SEQUENCING Cytochrome P450 2D6 Genotyping (CYP2D6 - Alleles) Peripheral blood - 7-8 days
56 BGSNG16 SANGERS SEQUENCING SANGER SEQUENCING Cystic Fibrosis mutation screening (CFTR - Del 508 ) Peripheral blood - 7-8 days
57 BGSNG15 SANGERS SEQUENCING Cystic Fibrosis mutation screening (CFTR - Del 508)[Prenatal ] Amniotic fluid / Chorionic villi / Cord blood +EDTA blood of mother - 7-8 days
58 BGSNG14 SANGERS SEQUENCING Criggler Najjar Syndrome Peripheral Blood - 7-8 days
59 BGSNG13 SANGERS SEQUENCING Colorectal Cancer Panel [NRAS,KRAS,BRAF] Tumor tissue - 7-8 days
60 BGSNG12 SANGERS SEQUENCING Chronic Neutrophilic Leukemia (CNL)(CSF3R gene exon 14 & 17; SETBP gene - exon 4) Bone Marrow/Peripheral Blood - 7-8 days
61 BGSNG11 SANGERS SEQUENCING cKIT Mutation Screening (Exons 9, 11, 13, 17) AML Peripheral blood - 7-8 days
62 BGSNG10 SANGERS SEQUENCING CEBPA Full Gene Mutation Peripheral Blood - 5-6 days
63 BGSNG09 SANGERS SEQUENCING CALR Mutation Analysis (Deletion or Insertion in Exon 9) Bone Marrow/Peripheral Blood - 7-8 days
64 BGSNG08 SANGERS SEQUENCING BRAF Mutation Analysis (V600E) Tumor tissue - 7-8 days
65 BGSNG07 SANGERS SEQUENCING Beta Thalassemia-HBB Full Gene Analysis (Couple + Prenatal) [TRIO ANALYSIS] Amniotic fluid / Chorionic villi / Cord blood + WB -EDTA of parents - 8-10 days
66 BGSNG06 SANGERS SEQUENCING Beta Thalassemia-HBB Full gne - Couple Peripheral blood - 8-10 days
67 BGSNG05 SANGERS SEQUENCING Beta Thalassemia-HBB Full gne - Single Peripheral blood - 8-10 days
68 BGSNG04 SANGERS SEQUENCING BCR-ABL1 Kinase Domain Mutations (IRMA) Bone marrow / Peripheral blood - 20-21 days
69 BGSNG03 SANGERS SEQUENCING AML Extended Panel (BCR/ABL,AML/ETO, CBFB, PML/RARA, FLT3, NPM1, CEBPA) Bone marrow / Peripheral blood - 7-8 days
70 BGSNG02 SANGERS SEQUENCING Achondroplasia (FGFR3 full gene sequence analysis) Peripheral blood/Amniotic Fluid/ Chorionic villi/ Cord blood - 2-3 weeks
71 BGSNG01 SANGERS SEQUENCING Sangers Achondroplasia Mutation Analysis (FGFR3 gene G1138A, G1138C) Peipheral blood DAILY 10-12 days
72 BGSNG69 SANGERS SEQUENCING Sangers C KIT MUTATIONS - EXONS 9,11, 13, 17 WB EDTA DAILY 5 DAYS