General Oncology
DNA Labs India | Diagnostic Tests
General Oncology
Clinical Overview
Sub-category mapping under Genetics & Genomics
| Reviewed by: Dr. Rajesh Kumar, MD Pathology | ISO 9001:2015 Certified Laboratory
This content is for educational purposes only. Always consult a qualified healthcare provider for medical advice.
Tests
DPD Gene Mutations (5-FU Toxicity) Detection Test
To detect mutations in the DPD gene that increase the risk of severe toxicity from 5-fluorouracil (5...
T-Cell Gene Rearrangement Mutation Detection Test
This assay is useful to diagnose a lymphoma, monitor the progress of treatment of lymphoma, and meas...
5-Fluorouracil (5FU) Toxicity Test
The primary purpose of the 5FU Toxicity Test is to detect DPYD gene polymorphisms that cause partial...
BCR-ABL Gene Rearrangement PCR Qualitative Test
To qualitatively detect the BCR-ABL gene rearrangement for diagnosing and monitoring chronic myeloid...
CALR Mutation Detection Test
The primary purpose of the CALR Mutation Detection Test is to diagnose myeloproliferative neoplasms...
Cancer Targeted Gene Panel: Lung Test
The purpose of this test is to analyze specific genes and mutations associated with lung cancer, suc...
Chromosome Analysis Philadelphia Test
The primary purpose of the Chromosome Analysis Philadelphia Test is to identify the presence of the...
C-KIT Mutation Detection PCR Test
To detect mutations in the C-KIT gene for early diagnosis of associated cancers, inform prognosis, a...
FISH - ALK-1 Breakapart Rearrangement Test
To detect ALK gene rearrangement in cancer cells for accurate diagnosis and treatment planning in no...
FISH - BCR / ABL or Philadelphia Translocation Test
To diagnose Chronic Myelogenous Leukemia (CML) and other leukemias associated with the Philadelphia...
FISH - MET (7q31) Amplification Test
The purpose of the FISH - MET (7q31) Amplification Test is to identify amplifications in the MET gen...
FISH - MDS Panel - Chromosomes 5q, 7q, 8q & 20q Test
The primary purpose of the FISH MDS Panel is to identify recurrent chromosomal abnormalities associa...
FISH - RARA (17q21) Variant Translocation Test
The purpose of this test is to detect variant RARA gene translocations that are not identified by st...
Genetic Mapping for Oncology / Cancer Test
The purpose of genetic mapping for oncology is to detect inherited genetic mutations that elevate ca...
Imatinib Resistance Mutation Analysis IRMA Test
The primary purpose of the IRMA test is to identify genetic mutations that confer resistance to Imat...
Inv16 (p13q22) / t(1616)(p13q22) Gene Rearrangement Qualitative PCR Test
The primary purpose of the Inv16 gene rearrangement qualitative PCR test is to detect the presence o...
JAK 2 Mutation Detection Qualitative PCR Test
The primary purpose of the JAK2 Mutation Detection Qualitative PCR Test is to detect the presence or...
JAK 2 V617F CALR & MPL Mutation Detection Profile Test
This test is ordered to detect the presence of JAK2 V617F, CALR, or MPL gene mutations, which are ha...
Medullary Thyroid Carcinoma Mutation Detection Test
The purpose of this test is to detect mutations in the RET gene to identify individuals at high risk...
NPM1 Gene Mutation Test
To detect mutations in the NPM1 gene associated with acute myeloid leukemia for diagnosis, prognosis...
Nx Gen Sequencing: Hereditary Retinoblastoma Test
The purpose of the Nx Gen Sequencing test for hereditary retinoblastoma is to identify pathogenic mu...
Oncomine Chronic Myelomonocytic Leukaemia (CMML) Panel Test
The purpose of the Oncomine CMML Panel Test is to identify genetic mutations and fusion genes in pat...
Oncomine Myelodysplastic Syndrome (MDS) Panel Test
The purpose of this test is to identify genetic mutations in patients suspected of having myelodyspl...
Oncopro Comprehensive Cancer Panel: 161 Genes Test
This test is useful for elucidation of various mutations, copy number variations, gene fusions, and...
Oncomine Comprehensive Myeloid Panel Test
The primary purpose of the Oncomine Comprehensive Myeloid Panel Test is to identify somatic mutation...
Oncomine Juvenile Myelomonocytic Leukaemia (JMML) Panel Test
The primary purpose of the Oncomine JMML Panel Test is to detect pathogenic or likely pathogenic mut...
Oncopro Hereditary Cancer Risk Panel (Screens 200 Genes) Test
To screen for genetic mutations in 200 genes that increase the risk of hereditary cancers, based on...
t(11;19) (q23;p13.3) TCF3-BX1(E2A-PBX1) PCR Qualitative Test
To detect the presence of the TCF3-BX1 fusion gene for the diagnosis and management of leukemia and...
CACNA1S Gene Malignant hyperthermia type 5 NGS Genetic Test
The purpose of the CACNA1S Gene Malignant Hyperthermia Type 5 NGS Genetic Test is to diagnose malign...
BRIP1 Gene Fanconi anemia type J NGS Genetic Test
The purpose of this test is to confirm a diagnosis of Fanconi Anemia Type J by identifying mutations...
EXT1 Gene Chondrosarcoma, familial NGS Genetic Test
To detect mutations in the EXT1 gene associated with familial chondrosarcoma, aiding in diagnosis, r...
chr. 11p15 Gene Beckwith-Wiedemann syndrome NGS Genetic Test
To diagnose Beckwith-Wiedemann Syndrome by identifying genetic mutations in the chr. 11p15 gene, ass...
PTCH2 Gene Basal cell nevus syndrome due to germline PTCH2 mutation NGS Genetic Test
The purpose of the PTCH2 Gene Basal Cell Nevus Syndrome NGS Genetic Test is to detect germline mutat...
DNMT3A Gene Acute myeloid leukemia, somatic, DNMT3A related NGS Genetic Test
To identify DNMT3A gene mutations in AML patients for diagnosis, prognosis assessment, and personali...
Colon Cancer comprehensive panel NGS Genetic Test
The purpose of the Colon Cancer Comprehensive Panel NGS Genetic Test is to detect genetic mutations...
OncoDx panel NGS Genetic Test
To identify genetic mutations in cancer cells for accurate diagnosis, staging, and personalized trea...
SUFU Gene Basal cell nevus syndrome NGS Genetic Test
To diagnose Basal Cell Nevus Syndrome by detecting mutations in the SUFU gene using next-generation...
BRAF Gene BRAF, selective sequencing of exon 15 NGS Genetic Test
The purpose of this test is to identify mutations in exon 15 of the BRAF gene, which are critical fo...
PALB2 Gene Breast cancer, susceptibility to NGS Genetic Test
To identify mutations in the PALB2 gene that increase susceptibility to breast and ovarian cancer, e...
RAD51D Gene Breast-ovarian cancer, familial, susceptibility to, type 4 NGS Genetic Test
To detect mutations in the RAD51D gene that increase susceptibility to breast and ovarian cancer, en...
KCNQ1OT1 Gene Beckwith-Wiedemann syndrome NGS Genetic Test
The purpose of this test is to identify mutations or epigenetic alterations in the KCNQ1OT1 gene to...
RECQL Gene Breast cancer, susceptibility to NGS Genetic Test
The purpose of the RECQL Gene Breast Cancer Susceptibility NGS Genetic Test is to identify mutations...
PRKAR1A Gene Carney complex type 1 NGS Genetic Test
To detect mutations in the PRKAR1A gene for accurate diagnosis of Carney Complex Type 1, enabling ea...
SDHD Gene Carcinoid tumors, intestinal NGS Genetic Test
To detect mutations in the SDHD gene that increase the risk of intestinal carcinoid tumors for early...
RAD51C Gene Breast-ovarian cancer NGS Genetic Test
The purpose of the RAD51C Gene Breast-Ovarian Cancer NGS Genetic Test is to detect mutations in the...
RINT1 Gene Breast cancer, RINT1 related NGS Genetic Test
The purpose of the RINT1 Gene Breast Cancer NGS Genetic Test is to identify mutations in the RINT1 g...
CDC20 Gene Cell cycle disorder, CDC20 related NGS Genetic Test
To diagnose CDC20-related cell cycle disorders, assess cancer risk, and guide personalized treatment...
MSH6 Gene Colorectal cancer, hereditary nonpolyposis type 5 NGS Genetic Test
To identify mutations in the MSH6 gene associated with Hereditary Nonpolyposis Colorectal Cancer Typ...
MLH1 Gene Colorectal cancer, hereditary nonpolyposis type 2 NGS Genetic Test
The purpose of the MLH1 Gene NGS Genetic Test is to identify mutations in the MLH1 gene that cause h...
NRAS Gene Colorectal cancer, hereditary NGS Genetic Test
To identify mutations in the NRAS gene associated with hereditary colorectal cancer, enabling risk a...
EPCAM Gene Colorectal cancer, hereditary nonpolyposis type 8 NGS Genetic Test
The purpose of the EPCAM Gene NGS Genetic Test is to detect mutations in the EPCAM gene and other ge...
PMS2 Gene Colorectal cancer, hereditary nonpolyposis type 4 NGS Genetic Test
The purpose of this test is to detect pathogenic or likely pathogenic mutations in the PMS2 gene, wh...
MSH2 Gene Colorectal cancer, hereditary nonpolyposis type 1 NGS Genetic Test
The purpose of the MSH2 Gene NGS Genetic Test is to identify pathogenic mutations in the MSH2 gene t...
AKT1 Gene Cowden syndrome type 6 NGS Genetic Test
The purpose of the AKT1 Gene Cowden Syndrome Type 6 NGS Genetic Test is to detect mutations in the A...
MLH3 Gene Colorectal cancer, hereditary nonpolyposis type 7 NGS Genetic Test
The purpose of this test is to identify mutations in the MLH3 gene that are linked to hereditary col...
TGFBR2 Gene Colorectal cancer, hereditary nonpolyposis type 6 NGS Genetic Test
The purpose of the TGFBR2 Gene NGS Genetic Test is to identify pathogenic mutations in the TGFBR2 ge...
PIK3CA Gene Cowden syndrome type 5 NGS Genetic Test
To diagnose Cowden Syndrome Type 5 by detecting mutations in the PIK3CA gene using Next-Generation S...
CCND1 Gene Colorectal cancer, hereditary, susceptibility to NGS Genetic Test
The purpose of this test is to identify mutations in the CCND1 gene and other associated genes to as...
APC Gene Desmoid disease, hereditary NGS Genetic Test
The purpose of this test is to identify mutations in the APC gene that increase the risk of heredita...
SDHD Gene Cowden syndrome type 3 NGS Genetic Test
The SDHD Gene Cowden Syndrome Type 3 NGS Genetic Test is performed to identify mutations in the SDHD...
APC Gene Familial adenomatous polyposis coli NGS Genetic Test
The purpose of the APC Gene FAP NGS Genetic Test is to detect mutations in the APC gene that cause f...
RB1 Gene Hereditary Retinoblastoma NGS Genetic Test
The purpose of the RB1 Gene Hereditary Retinoblastoma NGS Genetic Test is to detect mutations in the...
NTHL1 Gene Familial adenomatous polyposis type 3 NGS Genetic Test
The purpose of the NTHL1 Gene FAP Type 3 NGS Genetic Test is to identify mutations in the NTHL1 gene...
EGFR Gene EGFR, selective sequencing of exons 18-21 NGS Genetic Test
The purpose of this test is to identify mutations in exons 18-21 of the EGFR gene, which are critica...
MUTYH Gene Familial adenomatous polyposis type 2 NGS Genetic Test
The purpose of the MUTYH Gene FAP Type 2 NGS Genetic Test is to identify pathogenic mutations in the...
MSH3 Gene Familial adenomatous polyposis type 4 NGS Genetic Test
To identify pathogenic mutations in the MSH3 gene for the diagnosis of Familial Adenomatous Polyposi...
IDH1 Gene IDH1, selective sequencing of exon 4 NGS Genetic Test
The purpose of the IDH1 Gene Exon 4 Sequencing Test is to detect mutations in exon 4 of the IDH1 gen...
RAD50 Gene Hereditary breast and ovarian cancer syndrome, RAD50 related NGS Genetic Test
The purpose of the RAD50 Gene NGS Genetic Test is to detect mutations in the RAD50 gene that are lin...
ANTXR1 Gene Hemangioma capillary infantile NGS Genetic Test
The purpose of this test is to identify mutations or alterations in the ANTXR1 gene that may be link...
JAK2 Gene JAK2, selective sequencing of exons 12, 14 and 16 NGS Genetic Test
To identify mutations in exons 12, 14, and 16 of the JAK2 gene for diagnosing myeloproliferative neo...
KDR Gene Hemangioma, capillary infantile, familial, susceptibility to NGS Genetic Test
The purpose of the KDR Gene Hemangioma NGS Genetic Test is to identify genetic mutations in the KDR...
IDH2 Gene IDH2, selective sequencing of exon 4 NGS Genetic Test
To identify mutations in exon 4 of the IDH2 gene using NGS technology for diagnosis, risk assessment...
CBL Gene Juvenile myelomonocytic leukemia, due to CBL germline mutation NGS Genetic Test
The purpose of the CBL Gene JMML NGS Genetic Test is to detect germline mutations in the CBL gene th...
SMAD4 Gene Juvenile polyposis/hereditary hemorrhagic telangiectasia syndrome NGS Genetic Test
To diagnose individuals at risk for Juvenile Polyposis/Hereditary Hemorrhagic Telangiectasia Syndrom...
RUNX1 Gene Leukemia, acute myeloid NGS Genetic Test
To identify mutations in the RUNX1 gene for diagnosis and personalized treatment of acute myeloid le...
PTPN11 Gene Leukemia, juvenile myelomonocytic NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the PTPN11 gene that cause juvenile...
EZH2 Gene Leukemia, lymphoblastic and myeloid, EZH2 related NGS Genetic Test
To detect mutations in the EZH2 gene that are associated with lymphoblastic and myeloid leukemia, ai...
CEBPA Gene Leukemia, acute myeloid, somatic NGS Genetic Test
The purpose of the CEBPA gene NGS test is to detect somatic mutations in the CEBPA gene associated w...
SMAD4 Gene Juvenile polyposis syndrome NGS Genetic Test
The purpose of the SMAD4 Gene Juvenile Polyposis Syndrome NGS Genetic Test is to identify mutations...
MC1R Gene Melanoma, cutaneous malignant NGS Genetic Test
To detect variations in the MC1R gene that may increase the risk of developing cutaneous malignant m...
CDK4 Gene Melanoma, cutaneous malignant, familial, CDK4 related NGS Genetic Test
To identify mutations in the CDK4 gene associated with familial melanoma, enabling early risk assess...
XRCC3 Gene Melanoma, cutaneous malignant, familial type 6, susceptibility to NGS Genetic Test
To identify mutations in the XRCC3 gene that increase the risk of developing familial melanoma, enab...
CDKN2A Gene Melanoma, cutaneous malignant, familial NGS Genetic Test
The purpose of this test is to detect mutations in the CDKN2A gene that are associated with an incre...
MITF Gene Melanoma, cutaneous malignant NGS Genetic Test
The purpose of this test is to detect mutations in the MITF gene that are associated with an increas...
POT1 Gene Melanoma, cutaneous malignant, familial type 10, susceptibility to NGS Genetic Test
The purpose of this test is to detect mutations in the POT1 gene that increase susceptibility to fam...
PDGFB Gene Meningioma, familial, PDGFB related NGS Genetic Test
The purpose of the PDGFB Gene Meningioma NGS Genetic Test is to identify mutations in the PDGFB gene...
SMARCE1 Gene Meningioma, familial, susceptibility to NGS Genetic Test
To identify mutations in the SMARCE1 gene for early detection, diagnosis, and management of familial...
MN1 Gene Meningioma, MN1 deficiency related NGS Genetic Test
The purpose of this test is to detect mutations or deficiencies in the MN1 gene using NGS technology...
SUFU Gene Meningioma, familial, susceptibility to NGS Genetic Test
To identify genetic mutations in the SUFU gene that increase the risk of developing familial meningi...
MSH2 Gene Mismatch repair cancer syndrome NGS Genetic Test
The purpose of this test is to identify mutations in the MSH2 gene that cause mismatch repair cancer...
MSH6 Gene Mismatch repair cancer syndrome NGS Genetic Test
To identify mutations in the MSH6 gene associated with mismatch repair cancer syndrome for risk asse...
MLH1 Gene Mismatch repair cancer syndrome NGS Genetic Test
The purpose of the MLH1 Gene Mismatch Repair Cancer Syndrome NGS Genetic Test is to detect mutations...
PMS2 Gene Mismatch repair cancer syndrome NGS Genetic Test
To identify mutations in the PMS2 gene for assessing hereditary cancer risk, guiding preventive care...
MMR genes Gene MMR genes methylation analysis NGS Genetic Test
To detect methylation changes in MMR genes for assessing cancer risk, aiding in early diagnosis, gen...
MLH1 Gene Muir-Torre syndrome NGS Genetic Test
The purpose of this test is to identify mutations in the MLH1 gene that cause Muir-Torre syndrome an...
TET2 Gene Myelodysplastic syndrome, somatic NGS Genetic Test
The purpose of the TET2 Gene Myelodysplastic Syndrome NGS Genetic Test is to identify somatic mutati...
JAK2 Gene Myelofibrosis, somatic NGS Genetic Test
The purpose of this test is to identify somatic mutations in the JAK2 gene associated with myelofibr...
NF2 Gene Neurofibromatosis type 2 NGS Genetic Test
To detect mutations in the NF2 gene for diagnosis of Neurofibromatosis type 2, aiding in clinical ma...
NF1 Gene Neurofibromatosis type 1 NGS Genetic Test
The purpose of the NF1 Gene Neurofibromatosis Type 1 NGS Genetic Test is to identify mutations in th...
NRAS Gene NRAS, selective sequencing of exons 2 and 3 NGS Genetic Test
To identify mutations in exons 2 and 3 of the NRAS gene, which are associated with an increased risk...
SDHD Gene Paraganglioma and gastric stromal sarcoma NGS Genetic Test
The purpose of this test is to detect mutations in the SDHD gene that may indicate a predisposition...
SDHD Gene Paragangliomas type 1, with or without deafness NGS Genetic Test
To identify mutations in the SDHD gene for the diagnosis of Paragangliomas Type 1, with or without d...
SDHB Gene Paragangliomas type 4 NGS Genetic Test
To identify mutations in the SDHB gene that cause paragangliomas type 4, aiding in diagnosis, risk a...
CDKN2A Gene Pancreatic cancer/melanoma syndrome, familial NGS Genetic Test
The purpose of the CDKN2A Gene Pancreatic Cancer/Melanoma Syndrome NGS Genetic Test is to identify m...
SDHAF2 Gene Pheochromocytoma type 5 NGS Genetic Test
The purpose of this test is to identify mutations in the SDHAF2 gene for early detection and managem...
TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test
The purpose of the TMEM127 Gene Pheochromocytoma type 8 NGS Genetic Test is to identify mutations in...
SDHB Gene Pheochromocytoma type 2 NGS Genetic Test
To identify mutations in the SDHB gene that are associated with Pheochromocytoma type 2, enabling ea...
SDHD Gene Pheochromocytoma type 1 NGS Genetic Test
To identify mutations in the SDHD gene for diagnosis, risk assessment, and management of Pheochromoc...
MAX Gene Pheochromocytoma type 9 NGS Genetic Test
To identify genetic mutations in the MAX gene that cause pheochromocytoma type 9, aiding in diagnosi...
5-Flurouracil (5-FU) Toxicity and Chemotherapeutic Response (DPYD Variants)
To identify DPYD gene variants that affect the metabolism of 5-fluorouracil, helping to predict toxi...
MET Gene Renal cell carcinoma, papillary type 1, familial NGS Genetic Test
To detect pathogenic mutations in the MET gene associated with familial papillary renal cell carcino...
RNASEL Gene Prostate cancer, hereditary type 1 NGS Genetic Test
The purpose of this test is to detect mutations in the RNASEL gene, specifically the R462Q mutation,...
BRAF Mutation Analysis (V600E)
The purpose of BRAF Mutation Analysis (V600E) is to identify the presence of the BRAF V600E mutation...
CBFB-MYH11[Inv(16)] Qualitative
The primary purpose of the CBFB-MYH11[Inv(16)] Qualitative Test is to confirm the diagnosis of AML w...
cKIT Mutation Screening (Exons 9, 11, 13, 17) Gastrointestinal Stromal Tumors
The purpose of cKIT mutation screening is to detect mutations in exons 9, 11, 13, and 17 of the cKIT...
CEBPA Full Gene Mutation Analysis
The purpose of CEBPA Full Gene Mutation Analysis is to detect mutations in the CEBPA gene, which are...
cKIT Mutation Screening (Exons 9, 11, 13, 17) AML
The purpose of cKIT mutation screening is to detect specific genetic mutations in the cKIT gene that...
Chronic Neutrophilic Leukemia (CNL)(CSF3R Gene - Exon 14 & 17; SETBP Gene - Exon 4)
The purpose of this genetic test is to identify specific mutations in the CSF3R and SETBP genes asso...
Comprehensive Hereditary Cancer Panel (154 Genes)
To identify genetic mutations associated with hereditary cancer syndromes for risk assessment and pr...
CXCR4 Gene Mutation Analysis
The purpose of CXCR4 gene mutation analysis is to detect mutations in the CXCR4 gene, which can help...
EWSR1 Gene (Ewing's Sarcoma)
The purpose of EWSR1 gene testing is to identify genetic alterations, specifically EWSR1 gene fusion...
FLT3/ITD Allelic Ratio
The primary purpose of the FLT3/ITD Allelic Ratio Test is to identify the presence and quantify the...
HBOC Extended Panel [Hereditary Breast And Ovarian Cancer] (32 Genes)
The purpose of the HBOC Extended Panel test is to identify inherited mutations in 32 genes linked to...
Iamp (21)
To detect abnormalities in chromosome 21 for diagnosing genetic disorders such as Down syndrome, Edw...
IDH1 & IDH2 Mutation Analysis
The purpose of IDH1 & IDH2 mutation analysis is to diagnose mutations in the IDH1 and IDH2 genes, wh...
IGVH Mutation Load
The purpose of the IGVH Mutation Load Test is to assess the mutation status of the IGVH gene, which...
Irnotecan Toxicity Assessment (UGT1A1 Genotyping)/ Gilbert Syndrome
To assess the risk of irnotecan toxicity in patients undergoing chemotherapy and to identify individ...
KRAS,NRAS
The purpose of KRAS and NRAS gene testing is to identify mutations in these oncogenes, which are cru...
DNA Genetic Methylation Test
To determine the methylation status of the MGMT promoter gene for prognosis in glioblastoma and to a...
Microsatellite Instability (Lynch Syndrome/Colorectal Cancer)
To detect microsatellite instability for the diagnosis of Lynch Syndrome and to assess the risk and...
Multiplex Panel (Cytogenetics & PCR for 28 translocations & 80 breakpoints) (CML, AML, ALL)
The purpose of this Multiplex Panel is to detect 28 different translocations and 80 breakpoints link...
Myeloproliferative Leukemia Mutation Screening (MPL - S505N; W515L)
The purpose of this test is to detect specific mutations in the MPL gene, namely S505N and W515L, wh...
MYD88 Gene Mutation Analysis
To detect mutations in the MYD88 gene for the diagnosis and management of associated diseases such a...
NGS Homologous Recombinant Deficiency [HRR] Panel
To detect homologous recombination deficiency (HRR) mutations associated with increased cancer risk...
Nervous System Cancer Gene Panel
To identify genetic mutations in genes linked to nervous system cancers, aiding in diagnosis, progno...
NGS TP53 Mutation Analysis
The purpose of NGS TP53 Mutation Analysis is to identify pathogenic variants in the TP53 gene that m...
NPM1 Gene Fragment Analysis
The purpose of NPM1 Gene Fragment Analysis is to identify mutations in the NPM1 gene, which are biom...
NRAS Mutation Analysis (Codons 12 & 13)
The purpose of NRAS Mutation Analysis (Codons 12 & 13) is to identify specific genetic mutations in...
NPM1 Mutation Analysis (Exon 12 Insertion)
To detect NPM1 gene mutations for AML diagnosis and prognosis, aiding in treatment decisions and ris...
MLL t(4;11)(q21;q23) Qualitative
The purpose of the MLL t(4;11)(q21;q23) qualitative test is to detect the presence of the chromosoma...
NPM1+FLT3+CEBPA
The purpose of the NPM1+FLT3+CEBPA genetic test is to identify mutations in the NPM1, FLT3, and CEBP...
Oncomine Comprehensive Plus Panel
The purpose of the Oncomine Comprehensive Plus Panel is to provide detailed genetic profiling of can...
Oncomine Tumor Mutation Burden (TMB)
The purpose of the Oncomine TMB test is to predict the response of cancer patients to immunotherapy...
Oncomine Lung cfTNA Cancer Panel
To detect lung cancer-related genetic mutations in circulating tumor DNA (ctDNA) from blood, aiding...
Oncomine Myeloid Panel [MDS,MPN,AML,CML,CMML,JMML]
The purpose of the Oncomine Myeloid Panel is to detect genetic mutations associated with myeloid mal...
Pancreatic Mutation Panel
The purpose of the Pancreatic Mutation Panel test is to detect inherited genetic mutations linked to...
PDGFR + cKIT (Gastrointestinal Stromal Tumors)
The purpose of PDGFR + cKIT testing is to identify mutations in the PDGFR and cKIT genes associated...
PDGFR Mutation Screening (Exons 12, 14, 18)
The purpose of PDGFR mutation screening is to detect mutations in exons 12, 14, and 18 of the PDGFR...
PIK3CA Mutation Analysis (Exon 7, 9 & 20)
The purpose of PIK3CA Mutation Analysis is to identify genetic mutations in the PIK3CA gene that may...
PML/RARA Qualitative [BCR 1 & 3]
To detect the PML/RARA fusion gene for diagnosing Acute Promyelocytic Leukemia (APL).
PIK3CA by NGS
The purpose of the PIK3CA by NGS test is to identify mutations in the PIK3CA gene, which are associa...
Pediatric ALL Panel - Karyotyping + MLPA Deletion/Duplication + FISH Panel
The purpose of the Pediatric ALL Panel is to detect and characterize the genetic abnormalities assoc...
Replication Factor C1 Mutation Screening (RFC1 - 80G>A)
To screen for the RFC1-80G>A mutation to assess the risk of developing breast, ovarian, colorectal,...
Sarcoma Gene Panel
The purpose of the Sarcoma Gene Panel is to identify genetic mutations that increase the risk of sar...
RUNX1-RUNX1T1 (AML1- ETO) t(8;21) Quantitative
The RUNX1-RUNX1T1 Quantitative Test is performed to detect and measure the level of the RUNX1-RUNX1T...
TEL/AML1 Qualitative
The purpose of the TEL/AML1 qualitative test is to identify the genetic abnormality responsible for...
TEL/AML1 Quantitative
To detect and quantify the TEL/AML1 fusion gene for diagnosing TEL/AML1-positive acute lymphoblastic...
BCR/ABL Minor Quantitative Test
The purpose of the BCR/ABL Minor Quantitative Test is to detect and measure the BCR/ABL fusion gene...
FISH - Follicular Lymphoma (IGH/BCL2) t(14;18) Test
The test detects the IGH/BCL2 t(14;18) translocation by FISH to confirm the diagnosis of follicular...
Comprehensive Hereditary Cancer Panel (190 Genes) Test
This 190-gene panel helps identify inherited pathogenic variants that increase the risk of hereditar...
PIK3CA Mutation Analysis Test
The purpose of this test is to identify mutations in the PIK3CA gene from tumor tissue. This informa...
WT-1 Mutation Detection Test
The primary purpose of the WT-1 mutation detection test is to detect germline mutations in the WT1 g...
ATR Gene Cutaneous telangiectasia and cancer syndrome, familial NGS Genetic Test
To diagnose mutations in the ATR gene for Cutaneous Telangiectasia and Cancer Syndrome, Familial, ai...
MTAP Gene Diaphyseal medullary stenosis with malignant fibrous histiocytoma NGS Genetic Test
To identify mutations in the MTAP gene for diagnosis of diaphyseal medullary stenosis with malignant...
ERCC4 Gene Fanconi anemia, complementation group Q NGS Genetic Test
The purpose of this test is to detect mutations in the ERCC4 gene associated with Fanconi anemia, co...
RHBDF2 Gene Tylosis with esophageal cancer NGS Genetic Test
To identify pathogenic mutations in the RHBDF2 gene associated with tylosis and increased risk of es...
WT1 Gene Wilms tumor type 1, familial NGS Genetic Test
The purpose of this test is to detect mutations in the WT1 gene for early diagnosis of familial Wilm...
MDM2 Gene Accelerated tumor formation, susceptibility to NGS Genetic Test
To identify mutations in the MDM2 gene that increase susceptibility to accelerated tumor formation a...
PTCH1 Gene Basal cell nevus syndrome NGS Genetic Test
To diagnose Basal Cell Nevus Syndrome (Gorlin Syndrome) by detecting pathogenic mutations in the PTC...
FLCN Gene Birt-Hogg-Dube syndrome NGS Genetic Test
To detect pathogenic mutations in the FLCN gene for diagnosis, risk assessment, and management of Bi...
POLE Gene FILS syndrome NGS Genetic Test
To identify mutations in the POLE gene for diagnosing POLE Gene FILS Syndrome, assessing cancer risk...
ALK Gene Neuroblastoma type 3, susceptibility to, familial NGS Genetic Test
The purpose of this test is to identify germline mutations in the ALK gene that predispose to famili...
Breast Cancer BRCA1 BRCA2 Gene Test
The primary purpose of this test is to assess an individual's inherited risk of developing breast an...
CDH1 Gene Gastric cancer, hereditary diffuse NGS Genetic Test
The purpose of this test is to identify pathogenic variants in the CDH1 gene that are associated wit...
NDUFA13 Gene Hurthle cell thyroid carcinoma, due to germline NDUFA13 mutation NGS Genetic Test
The purpose of this NGS genetic test is to identify germline mutations in the NDUFA13 gene that are...
KIT Gene Gastrointestinal stromal tumor, familial NGS Genetic Test
The primary purpose of this NGS genetic test is to detect inherited (germline) mutations in the KIT...
PAX5 Gene Leukemia, acute lymphoblastic, susceptibility to, due to PAX5 germline mutation NGS Genetic Test
The purpose of this NGS genetic test is to detect germline mutations in the PAX5 gene that increase...
KRAS Gene Leukemia, acute myelogenous NGS Genetic Test
The purpose of this NGS genetic test is to detect mutations in the KRAS gene that are associated wit...
CEBPA Gene Leukemia, myeloid acute form, due to CEBPA germline mutation NGS Genetic Test
The purpose of this NGS genetic test is to detect germline mutations in the CEBPA gene that predispo...
KIT Gene Leukemia, acute myeloid NGS Genetic Test
The purpose of this test is to identify mutations in the KIT gene that are associated with acute mye...
TP53 Gene Li-Fraumeni syndrome type 1 NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the TP53 gene that are associated wi...
SUFU Gene Medulloblastoma, desmoplastic, familial NGS Genetic Test
The purpose of this test is to detect mutations in the SUFU gene that are associated with desmoplast...
CHEK2 Gene Li-Fraumeni syndrome type 2 NGS Genetic Test
The primary purpose of this test is to identify pathogenic variants in the CHEK2 gene that are assoc...
RET Gene Multiple endocrine neoplasia type 2A NGS Genetic Test
The purpose of this test is to identify disease-causing mutations in the RET gene to confirm a diagn...
CDKN2A Gene Melanoma and neural system tumor syndrome, familial NGS Genetic Test
The purpose of this test is to identify mutations in the CDKN2A gene that predispose individuals to...
RET Gene Multiple endocrine neoplasia type 2B NGS Genetic Test
The purpose of this test is to detect pathogenic mutations in the RET gene that cause Multiple Endoc...
NPM1 Gene NPM1, selective sequencing of exon 11 NGS Genetic Test
The purpose of this test is to detect mutations in exon 11 of the NPM1 gene, which are frequently fo...
PDGFRA Gene PDGFRA, selective sequencing of exons 12, 14 and 18 NGS Genetic Test
The purpose of this test is to detect mutations in exons 12, 14, and 18 of the PDGFRA gene, which ar...
AIP Gene Pituitary adenoma, growth hormone-secreting, due to AIP germline mutation NGS Genetic Test
The purpose of this test is to confirm the diagnosis of growth hormone-secreting pituitary adenoma c...
AIP Gene Pituitary adenoma, prolactin-secreting, due to AIP germline mutation NGS Genetic Test
The purpose of this NGS genetic test is to identify germline mutations in the AIP gene that are asso...
JAK2 Gene Polycythemia vera, somatic NGS Genetic Test
The purpose of this test is to detect somatic mutations in the JAK2 gene that are associated with po...
DICER1 Gene Pleuropulmonary blastoma NGS Genetic Test
The primary purpose of this test is to identify pathogenic mutations in the DICER1 gene that increas...
HOXB13 Gene Prostate cancer, familial, association with NGS Genetic Test
The purpose of this test is to identify pathogenic variants in the HOXB13 gene that are associated w...
HNF1A Gene Renal cell carcinoma, due to HNF1A germline mutation NGS Genetic Test
The purpose of this test is to identify germline mutations in the HNF1A gene that are associated wit...
ELAC2 Gene Prostate cancer, hereditary type 2, susceptibility to NGS Genetic Test
The purpose of this test is to identify mutations in the ELAC2 gene that increase the risk of heredi...
RET Gene RET, selective sequencing of exons 5, 8, 10, 11 and 13-16 NGS Genetic Test
The purpose of this test is to identify pathogenic variants in the RET gene that predispose individu...
CYLD Gene Spiegler-Brooke syndrome NGS Genetic Test
The purpose of this test is to identify pathogenic mutations in the CYLD gene that cause Spiegler-Br...
SRGAP1 Gene Thyroid cancer type 2, nonmedullary, susceptibility to NGS Genetic Test
The purpose of this NGS genetic test is to detect mutations in the SRGAP1 gene that are associated w...
ARL11 Gene Tumor predisposition syndrome, ARL11 related NGS Genetic Test
The purpose of this test is to detect mutations in the ARL11 gene that are associated with tumor pre...
BAP1 Gene Tumor predisposition syndrome NGS Genetic Test
The primary purpose of this NGS genetic test is to detect pathogenic mutations in the BAP1 gene that...
RHBDF2 Gene Tylosis with esophageal cancer NGS Genetic Test
The primary purpose of this NGS genetic test is to identify mutations in the RHBDF2 gene that cause...
VHL Gene von Hippel-Lindau syndrome NGS Genetic Test
The purpose of the VHL Gene NGS Genetic Test is to confirm or rule out a diagnosis of Von Hippel-Lin...
E2A t(1;19)(q23;p13) Qualitative
The purpose of this test is to detect the E2A-PBX1 fusion gene resulting from the t(1;19) translocat...
Endocrine Cancer Gene Panel
The purpose of the Endocrine Cancer Gene Panel is to identify inherited genetic mutations that predi...
PML/RARA Quantitative Test
The primary purpose of the PML/RARA quantitative test is to detect the presence of the PML-RARA fusi...
Thyroid Prognostication NGS Panel
The primary purpose of the Thyroid Prognostication NGS Panel is to provide prognostic information fo...
Hereditary Cancer Panel
The purpose of the Hereditary Cancer Panel is to identify inherited genetic mutations that increase...
Predictive Genetic Testing for Cancer
The purpose of predictive genetic testing for cancer is to identify inherited genetic mutations that...