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| Test # | Test Name | Test Keywords | Additional Information |
|---|---|---|---|
| 3001309 | 1p/19q Deletion by FISH | 1p19q, Oncology, Paraffin, Brain Tumors, Tumor | Additional Technical Information |
| 2002647 | Acute Lymphocytic Leukemia (ALL) Panel by FISH, Adult | FISH A ALL, B-Cell Lymphoma, MYC BCR-ABL1, MLL, IGH@, TCF3, E2A | |
| 2002719 | Acute Lymphocytic Leukemia (ALL) Panel by FISH, Pediatric | FISH P ALL, Oncology, Bone Marrow , B-Cell Lymphoma, childhood, child, children, CEP4, CEP10, BCR-ABL1 MLL, ETV6-RUNX1, TEL-AML1 | |
| 2002653 | Acute Myelogenous Leukemia (AML) with Myelodysplastic Syndrome (MDS), or Therapy-Related AML, by FISH | F TAML MDS, Myelodysplastic syndrome, Acute Myeloid Leukemia, EGR1, D7S486, MLL | |
| 2011132 | Acute Myelogenous Leukemia Panel by FISH | FISH AML P, Acute Myeloid Leukemia, AML, Myeloproliferative, MPD, PML-RARA, RUNX1T1-RUNX1, ETO-AML1, CBFB, MLL, RPN1/MECOM, EVI1, EGR1, D7S486, KMT2A | |
| 2011431 | ALK (D5F3) by Immunohistochemistry with Reflex to ALK Gene Rearrangements by FISH | ||
| 2007324 | ALK (D5F3) with Interpretation by Immunohistochemistry | ALKD5F3 IP | Additional Technical Information |
| 3001302 | ALK Gene Rearrangements by FISH, Lung | ALK GENE, Lung cancer, pharmcogenetics, pulmonary cancer | |
| 2006193 | B-Cell Clonality Screening (IgH and IgK) by PCR | B-Cell Lymphomas, B-cell Leukemias | Additional Technical Information |
| 2008420 | BCR-ABL1 Mutation Analysis by Next Generation Sequencing | Chronic Myelogenous Leukemia (CML), Acute Lymphoblastic Leukemia (ALL), Tumor Markers, NGS | Additional Technical Information |
| 2005017 | BCR-ABL1, Major (p210), Quantitative | Acute Lymphoblastic Leukemia (ALL), Chronic Myelogenous Leukemia (CML) | |
| 2005016 | BCR-ABL1, Minor (p190), Quantitative | Acute Lymphoblastic Leukemia (ALL), Chronic Myelogenous Leukemia (CML) | |
| 2005010 | BCR-ABL1, Qualitative with Reflex to BCR-ABL1 Quantitative | Chronic Myelogenous Leukemia (CML) | |
| 2007130 | Bone Marrow, Chromosome Analysis with Reflex to Genomic Microarray | ALL, Bcell, B-cell, b cell, T-cell, Tcell, T Cell, B-ALL, CDKN2A/B, BTG1, IKZF1, EBF1, UPD 9p, Myelodysplastic, MDS, Myeloproliferative, MPD, 5q-; -7 or 7q-,+8; 20q-, LOH, UPD 7q, UPD 11q, UPD 17p, CLL, P53, Chronic lymphocytic leukemia | |
| 2002498 | BRAF codon 600 Mutation Detection by Pyrosequencing | Melanoma, Colorectal cancer, Lynch Syndrome, HNPCC, Hereditary Nonpolyposis Colorectal Cancer, Gastrointestinal Adenocarcinoma, Papillary thyroid carcinoma | |
| 0051750 | BRAF Codon 600 Mutation Detection with Reflex to MLH1 Promoter Methylation | BRAF RFLX, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, Lynch Syndrome, Tumor Markers | |
| 2013921 | BRAF V600E Mutation Detection in Circulating Cell-Free DNA by Digital Droplet PCR | ||
| 2007132 | BRAF V600E Mutation Detection in Hairy Cell Leukemia by Real-Time PCR, Quantitative | Additional Technical Information | |
| 2011954 | Breast and Ovarian Hereditary Cancer Syndrome (BRCA1 and BRCA2) Sequencing | BRCA FGS, BRACA, HBOC | |
| 2011949 | Breast and Ovarian Hereditary Cancer Syndrome (BRCA1 and BRCA2) Sequencing and Deletion/Duplication | BRCA FGA, BRACA, HBOC | |
| 2010673 | CALR (Calreticulin) Exon 9 Mutation Analysis by PCR | ||
| 2011114 | CBFB-MYH11 inv(16) Detection, Quantitative | Acute Myeloid Leukemia (AML), Tumor Markers | Additional Technical Information |
| 2004247 | CEBPA Mutation Detection | Acute Myelogenous Leukemia (AML) | Additional Technical Information |
| 2002295 | Chromosome FISH, CLL Panel | FISH CLLP, Chronic Lymphocytic Leukemia, CLL, Lymphoma Phenotyping, B-Cell Lymphomas, Tumor Markers, ATM, D12Z3, D13S319, TP53, p53 | |
| 2002298 | Chromosome FISH, Interphase | Oncology, Bone Marrow, Ewing Sarcoma, Neuroblastoma, Myelodysplastic, MDS, Chronic Lymphocytic Leukemia (CLL), Sarcoma, Acute Lymphoblastic Leukemia (ALL), Chronic Myelogenous Leukemia (CML), Tumor Markers, Acute Myeloid Leukemia (AML), Myeloproliferative Neoplasms (MPN), Plasma Cell Dyscrasias, Lymphoma Phenotyping, B-Cell Lymphomas | Please specify which FISH probe you wish to order. |
| 2010229 | Cytogenomic Molecular Inversion Probe Array, Copy Number and Heterozygosity Assessment - Formalin-Fixed Paraffin-Embedded (FFPE) Tissue | FFPE ARRAY, array CGH; aCGH; Array Comparative Genomic Hybridization; Chromosomal Microarray; CMA; CGH; Microarray; Single-nucleotide-polymorphism (SNP) array; Whole Genome Array; tumor; oncology, formalin-fixed, paraffin-embedded, FFPE; tissue | |
| 2006325 | Cytogenomic SNP Microarray—Oncology | CMA ONC ALL, Bcell, B-cell, b cell, T-cell, Tcell, T Cell, B-ALL, CDKN2A/B, BTG1, IKZF1, EBF1, UPD 9p, Myelodysplastic, MDS, Myeloproliferative, MPD, 5q-; -7 or 7q-,+8; 20q-, LOH, UPD 7q, UPD 11q, UPD 17p, CLL, P53, Chronic lymphocytic leukemia | Additional Technical Information |
| 3001304 | DDIT3 (CHOP) (12q13) Gene Rearrangement by FISH | CHOPFISH, Sarcoma, myxoid liposarcoma, round cell liposarcoma | Additional Technical Information |
| 2012166 | Dihydropyrimidine Dehydrogenase (DPYD) Genotyping, 3 Mutations | DYPD 5-Fluorouracil toxicity 5-FU toxicity 5-FU toxicity 5FU toxicity Adrucil (DPYD) Genotyping, 3 Mutations Xeloda (capecitabine) (DPYD) Genotyping, 3 Mutations DPD Uftoral (tegafur/uracil) (DPYD) Genotyping, 3 Mutations | |
| 0095155 | DNA Content/Cell Cycle Analysis, Miscellaneous | ||
| 3001310 | EGFR Gene Amplification by FISH | EGFRFISH, Head and Neck Cancer, Lung Cancer, Brain Tumors | Additional Technical Information |
| 2002440 | EGFR Mutation Detection by Pyrosequencing | Lung Cancer | Additional Technical Information |
| 2010696 | EIF2AK4-Associated Disorders (EIF2AK4) Sequencing | ||
| 2002378 | Eosinophilia Panel by FISH | FISH EOS P, Mast Cell Disease, Eosinophilic Diseases, Acute Myeloid Leukemia (AML), Myeloproliferative Neoplasms (MPN), PDGFRA-CHIC2-FIP1L1, PDGFRB, FGFR1, CBFB | |
| 2013906 | Epi proColon | ||
| 2007914 | EPOR Mutation Detection by Sequencing | Additional Technical Information | |
| 2002902 | Epstein-Barr Virus (EBV) by in situ Hybridization, Paraffin | Epstein-Barr Virus (EBV), Nasopharyngeal carcinoma, NK/ T-cell lymphomas, B-cell lymphomas, Post transplant lymphoproliferative disorders, Tumor Markers, ISH, Nasopharyngeal nonkeratinizing undifferentiated carcinoma, Nasal type NK/T-cell lymphoma | |
| 2008603 | ERBB2 (HER-2/neu) Gene Amplification by FISH, Tissue | HER2FISH, Breast Cancer, Tumor Markers, FISH, herceptin, HER2, HER-2, neu, HER2/neu, pathvision, pathvysion | |
| 2007332 | ERBB2 (HER2)(HercepTest) by Immunohistochemistry | HERCEP IHC | |
| 0049178 | ERBB2 (HercepTest®) by Immunohistochemistry, Tissue with Reflex to FISH if 2+ | Gastric, gastrointestinal cancer, tumor marker, pharmacogenetics, Breast Cancer, Tumor Markers, FISH, herceptin, HER2, HER-2, neu, HER2/neu, Pancreatic Cancer, Gastric Cancer, Barrett’s Esophagus Cancer, Gastroesophageal Junction Cancer | |
| 0049174 | ERBB2 (HercepTest®) with Interpretation by Immunohistochemistry, Tissue | Gastric, gastrointestinal cancer, tumor marker, pharmacogenetics, Breast Cancer, Tumor Markers, FISH, herceptin, HER2, HER-2, neu, HER2/neu, Pancreatic Cancer, Gastric Cancer, Barrett’s Esophagus Cancer, Gastroesophageal Junction Cancer | |
| 3001305 | EWSR1 (22q12) Gene Rearrangement by FISH | EWSR1, Ewing Sarcoma, Sarcoma, Tumor Markers | Additional Technical Information |
| 2004863 | Familial Adenomatous Polyposis (APC) Sequencing | APC FGS, Colorectal Cancer, colon cancer, CRC, polyps, Familial Adenomatious Polyposis FAP, familial cancer | |
| 2004915 | Familial Adenomatous Polyposis Panel: APC Sequencing, APC Deletion/Duplication, and MYH 2 Mutations | FAP Panel, Familial Adenomatious Polyposis familial cancer, Colorectal Cancer, colon cancer, CRC, polyps, FAP, familial cancer | |
| 2001961 | Familial Mutation, Targeted Sequencing | SEQ FSM |
The following genes are available: |
| 3001297 | FOXO1 (FKHR) (13q14) Gene Rearrangement by FISH | FKHRFISH, Sarcoma, FOX, FOXO1, 13q14, alveolar rhabdomyosarcoma | Additional Technical Information |
| 2002674 | Gastrointestinal Stromal Tumor Mutation | Gastrointestinal Stromal Tumors (GIST) | Additional Technical Information |
| 2012026 | Hereditary Breast and Ovarian Cancer Panel, Sequencing and Deletion/Duplication | BOCAPAN, Breast Cancer, Tumor Markers, FISH, ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MEN1, MLH1, MSH2, MSH6, MUTYH, NBN, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53 | |
| 2007108 | Hereditary Paraganglioma-Pheochromocytoma (SDHB) Sequencing and Deletion/Duplication | Additional Technical Information | |
| 2007167 | Hereditary Paraganglioma-Pheochromocytoma (SDHB, SDHC, and SDHD) Sequencing and Deletion/Duplication Panel | ||
| 2007117 | Hereditary Paraganglioma-Pheochromocytoma (SDHC) Sequencing and Deletion/Duplication | Additional Technical Information | |
| 2007122 | Hereditary Paraganglioma-Pheochromocytoma (SDHD) Sequencing and Deletion/Duplication | Additional Technical Information | |
| 0051650 | HNPCC/Lynch Syndrome (MLH1) Sequencing and Deletion/Duplication | MLH1 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch | |
| 0051654 | HNPCC/Lynch Syndrome (MSH2) Sequencing and Deletion/Duplication | MSH2 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch | Additional Technical Information |
| 0051656 | HNPCC/Lynch Syndrome (MSH6) Sequencing and Deletion/Duplication | MSH6 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch | Additional Technical Information |
| 0051737 | HNPCC/Lynch Syndrome (PMS2) Sequencing and Deletion/Duplication | PMS2 FGA, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch | Additional Technical Information |
| 2001728 | HNPCC/Lynch Syndrome Deletion/Duplication | HNPCC DD, Hereditary Nonpolyposis Colorectal Cancer, Colorectal Cancer, MLH1, MSH2, MSH6, PMS2, mismatch repair, Muir-Torre, Turcot, Lynch Syndrome | Additional Technical Information |
| 2007894 | Human Papillomavirus (HPV) Genotypes 16 and 18/45, E6/E7 mRNA by Transcription-Mediated Amplification (TMA) | ||
| 2007893 | Human Papillomavirus (HPV), High Risk, E6/E7 mRNA by Transcription-Mediated Amplification (TMA) | ||
| 2006444 | IDH1 and IDH2 Mutation Analysis, exon 4 | Gliomas, cytogenically normal AML cases | Additional Technical Information |
| 2007357 | IDH1 R132H Point Mutation with Interpretation by Immunohistochemistry | IDH1 IP | Additional Technical Information |
| 3001298 | IGH-BCL2 Fusion, t(14;18) by FISH for Detection in Follicular Lymphoma | B-Cell Lymphomas, Follicular lymphoma, Diffuse large B-cell lymphoma, FISH | Additional Technical Information |
| 3001306 | IGH-CCND1 Fusion, t(11;14) by FISH | Mantle cell lymphoma, B-Cell Lymphomas, Plasma cell dyscrasias, Tumor Markers | Additional Technical Information |
| 3001299 | IGH-MYC Fusion t(8;14) by FISH | Burkitt lymphoma, B-Cell Lymphomas | Additional Technical Information |
| 0040227 | IGHV Mutation Analysis by Sequencing | Chronic Lymphocytic Leukemia (CLL), Lymphoma Phenotyping, B-Cell Lymphomas, Tumor Markers | Additional Technical Information |
| 2002357 | JAK2 Exon 12 Mutation Analysis by PCR | Myeloproliferative Neoplasms (MPN), Tumor Markers | Additional Technical Information |
| 0051245 | JAK2 Gene, V617F Mutation, Qualitative | Myeloproliferative Neoplasms (MPN), Tumor Markers | Additional Technical Information |
| 2012084 | JAK2 Gene, V617F Mutation, Qualitative with Reflex to CALR (Calreticulin) Exon 9 Mutation Analysis by PCR with Reflex to MPL codon 515 Mutation Detection by Pyrosequencing, Quantitative | ||
| 2012085 | JAK2 Gene, V617F Mutation, Qualitative with Reflex to JAK2 Exon 12 Mutation Analysis by PCR | ||
| 0040168 | JAK2 Gene, V617F Mutation, Quantitation | Myeloproliferative Neoplasms (MPN), Tumor Markers | Additional Technical Information |
| 2004988 | Juvenile Polyposis (BMPR1A) Sequencing | BMPR1A FGS, JPS, SMAD4, Juvenile Polyposis | |
| 2004992 | Juvenile Polyposis (BMPR1A) Sequencing and Deletion/Duplication | BMPR1A FGA, JPS, SMAD4 | |
| 0051510 | Juvenile Polyposis (SMAD4) Sequencing | SMAD4 SEQ, Hereditary Hemorrhagic Telangiectasia (HHT), JP/HHT, BMPR1A, JPS, Myhre, Juvenile Polyposis | |
| 2001971 | Juvenile Polyposis (SMAD4) Sequencing and Deletion/Duplication | SMAD4 FGA, Hereditary Hemorrhagic Telangiectasia (HHT), JP/HHT, BMPR1A, JPS, Juvenile Polyposis | |
| 2002437 | KIT Mutations in AML by Fragment Analysis and Sequencing | Acute Myeloid Leukemia (AML), C-KIT, CKIT | Additional Technical Information |
| 2002695 | KIT Mutations, Melanoma | Melanoma, Tumor Markers, C-KIT, CKIT | Additional Technical Information |
| 2001932 | KRAS Mutation Detection with BRAF reflex | Pharmacogenetics (PGx), Lung Cancer, Colorectal Cancer, Tumor Markers, CRC, colon, rectal | Additional Technical Information |
| 2007131 | Leukemic Blood, Chromosome Analysis with Reflex to Genomic Microarray | ||
| 2008894 | Lung Cancer Panel | Panel consist of EFGR, ALK, ROS1, if ROS1 equivocal reflex to ROS1 FISH Additional Technical Information |
|
| 2008895 | Lung Cancer Panel with KRAS | Panel consist of EFGR, KRAS, ALK, ROS1, if ROS1 equivocal reflex to ROS1 FISH Additional Technical Information |
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| 2002650 | Lymphoma (Aggressive) Panel by FISH | FISH ALYMP, Lymphoma Phenotyping, B-Cell Lymphomas, Lymphoproliferative Disorders (LPD), BCL6, MYC, IGH@/BCL2 | Additional Technical Information |
| 3001301 | MDM2 Gene Amplification by FISH | MDM2 FISH, Sarcoma, Tumor Markers, MDM2, Murine Double Minute 2 | Additional Technical Information |
| 0055655 | Methylenetetrahydrofolate Reductase (MTHFR) 2 Mutations | MTHFR PCR, Thrombophilia, methotrexate sensitivity, cardiovascular, C677T, A1298C | |
| 2009310 | MGMT Methylation Detection by PCR | ||
| 0051740 | Microsatellite Instability (MSI), HNPCC/Lynch Syndrome, by PCR | MSI PCR, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, Lynch Syndrome, Tumor Markers, MSI, MLH1, MSH2, MSH6, PMS2, mismatch repair | Additional Technical Information |
| 0049302 | Mismatch Repair by Immunohistochemistry | MSI, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, Tumor Markers, MLH1, MSH2, MSH6, PMS2, mismatch repair, IHC, Lynch | Additional Technical Information |
| 2002327 | Mismatch Repair by Immunohistochemistry with Reflex to BRAF Codon 600 Mutation and MLH1 Promoter Methylation | Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, Tumor Markers, MSI, MLH1, MSH2, MSH6, PMS2, mismatch repair, IHC, Lynch | |
| 2005270 | Mismatch Repair by Immunohistochemistry with Reflex to MLH1 Promoter Methylation | MSI MLH1, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Colorectal Cancer, Tumor Markers, MLH1, MSH2, MSH6, PMS2, mismatch repair, IHC, Lynch | Additional Technical Information |
| 2002499 | MLH1 Promoter Methylation, Paraffin | MLH1PCR, Colorectal Cancer, Hereditary Nonpolyposis Colorectal Cancer, HNPCC, Tumor Markers | Additional Technical Information |
| 2005545 | MPL codon 515 Mutation Detection by Pyrosequencing, Quantitative | Myeloproliferative Neoplasms, MPN | Additional Technical Information |
| 2005359 | Multiple Endocrine Neoplasia Type 1 (MEN1) Sequencing | MEN1 FGS, Multiple endocrine adenomatosis, Wermer syndrome, Multiple Endocrine Neoplasias (MEN) | |
| 2005360 | Multiple Endocrine Neoplasia Type 1 (MEN1) Sequencing and Deletion/Duplication | MEN1 FGA, Multiple endocrine adenomatosis, Wermer syndrome, Multiple Endocrine Neoplasias (MEN) | |
| 0051390 | Multiple Endocrine Neoplasia Type 2 (MEN2), RET Gene Mutations by Sequencing | MEN2 SEQ, Thyroid Cancer, Pheochromocytoma, Multiple Endocrine Neoplasias (MEN), MEN 2A, MEN 2B, familial medullary thyroid carcinoma, FMTC, RET proto-oncogene | |
| 2002294 | Multiple Myeloma Panel by FISH | FISH MMP, Plasma Cell Dyscrasias, CKS1B, ASS1, CCND1-IGH@, IGH@, PML, TP53, FGFR3-IGH@, IGH@-MAF | |
| 3001300 | MYC (8q24) Gene Rearrangement by FISH | Burkitt lymphomas, B-Cell Lymphomas, Double Hit lymphomas, Tumor Markers | Additional Technical Information |
| 2009318 | MYD88 L265P Mutation Detection by PCR, Quantitative | Additional Technical Information | |
| 2002709 | Myelodysplastic Syndrome (MDS) Panel by FISH | FISH MDS P, Myelodysplastic Syndrome (MDS), EGR1, D7S486, CEP8, D20S108 | |
| 2011117 | Myeloid Malignancies Mutation Panel by Next Generation Sequencing | Additional Technical Information | |
| 2012182 | Myeloid Malignancies Somatic Mutation and Copy Number Analysis Panel | MYE CMANGS same as CMA ONC, MYE NGS | |
| 2002360 | Myeloproliferative Disorders Panel by FISH | FISH MPD P, Chronic Myelogenous Leukemia (CML), Myeloproliferative Neoplasms (MPN), PDGFRα-CHIC2-FIP1L1, PDGFRa-CHIC2-FIP1L1, PDGFRβ, FGFR1, ABL1-BCR | |
| 3000066 | NPM1 Mutation Detection by RT-PCR, Quantitative | Acute Myeloid Leukemia (AML) | Additional Technical Information |
| 2003123 | NRAS Mutation Detection by Pyrosequencing | Colorectal, melanoma, Hereditary Nonpolyposis Colorectal Cancer , HNPCC, Tumor Markers, CRC, colon, rectal | Additional Technical Information |
| 2010102 | PCA3 - Prostate Cancer Biomarker by Transcription-Mediated Amplification | Additional Technical Information | |
| 2008394 | Peutz-Jeghers Syndrome (STK11) Sequencing | STK11, STK11 FGS, hamartomatous polyps, mucocutaneous hypergigmentation | |
| 2008398 | Peutz-Jeghers Syndrome (STK11) Sequencing and Deletion/Duplication | STK11, STK11 FGA, hamartomatous polyps, mucocutaneous hypergigmentation | |
| 2002871 | PML-RARA Translocation, t(15;17) by RT-PCR, Quantitative | Acute Myelogenous Leukemia (AML), Acute Promyelocytic Leukemia (APL) | Additional Technical Information |
| 2002363 | PML/RARα Translocation by FISH | FISH PML, Acute Myeloid Leukemia (AML), Acute Promyelocytic Leukemia (APL), Tumor Markers | |
| 0080206 | Prostate Specific Antigen, Free Percentage (includes Free PSA and Total PSA), Serum or Plasma | Genitourinary Cancer, Prostate cancer, tumor marker | |
| 0070121 | Prostate Specific Antigen, Total, Serum or Plasma | Genitourinary Cancer, Prostate cancer, tumor marker | |
| 3001312 | RET Gene Rearrangements by FISH | ||
| 2008414 | ROS1 with Interpretation by Immunohistochemistry with Reflex to FISH if Equivocal or Positive | Additional Technical Information | |
| 2010138 | RUNX1-RUNX1T1 (AML1-ETO) t(8;21) Detection, Quantitative | ||
| 2006948 | SDHB with Interpretation by Immunohistochemistry | ||
| 2007991 | Solid Tumor Mutation Panel by Next Generation Sequencing | Additional Technical Information | |
| 3001303 | SS18 (SYT) (18q11) Gene Rearrangement by FISH | Additional Technical Information | |
| 0055567 | T-Cell Clonality Screening by PCR | Hematologic Cancer, Sézary Syndrome, T-Cell Lymphomas, Lymphoma Phenotyping | |
| 0092066 | Thiopurine Methyltransferase, RBC | TPMT RBC, Thiopurine Methyltransferase Activity (TPMT), Pharmacogenetics (PGx), Immunosuppressive Drugs, Rheumatoid Arthritis (RA), Inflammatory Bowel Disease (IBD) | Additional Technical Information |
| 0051332 | UDP Glucuronosyltransferase 1A1 (UGT1A1) Genotyping | UGT1A1, Irinotecan, Pharmacogenetics (PGx), Colorectal Cancer | |
| 2001181 | UroVysion FISH | UF, Bladder Cancer, Tumor Markers, urine |
