Molecular Oncology Tests: Test Categories



List of Test Request Forms
Alphabetically Test Categories Methodologies Diagnostic Categories Specimen Type

Test #
Test Name
1p/19q d(1:19) Deletion by FISH
AML1-ETO (RUNX1-RUNX1T1), t(8;21) Translocation by RT-PCR
API2-MLT1 (API2-MALT1), t(11;18) Translocation by RT-PCR
B-Cell and T-Cell Clonality Assessment by PCR, Fluid
B-Cell and T-Cell Clonality Assessment by PCR, Paraffin
B-Cell and T-Cell Clonality Assessment by PCR, Tissue
B-Cell and T-Cell Comprehensive Clonality Assessment, Fluid
B-Cell and T-Cell Comprehensive Clonality Assessment, Tissue
B-Cell Assessment by Restriction Fragment Southern Blot Hybridization, Fluid
B-Cell Clonality Assessment by Restriction Fragment-Southern Blot Hybridization, Tissue
B-Cell Clonality Screening Assay by PCR, Fluid
B-Cell Clonality Screening Assay by PCR, Paraffin
B-Cell Clonality Screening Assay by PCR, Tissue
bcl-1/JH (IGH-CCND1), t(11;14) Translocation by PCR, Fluid
bcl-1/JH (IGH-CCND1), t(11;14) Translocation by PCR, Paraffin
bcl-1/JH (IGH-CCND1), t(11;14) Translocation by PCR, Tissue
bcl-2/JH (IGH-BCL2), t(14;18) Translocation by PCR, Fluid
bcl-2/JH (IGH-BCL2), t(14;18) Translocation by PCR, Paraffin
bcl-2/JH (IGH-BCL2), t(14;18) Translocation by PCR, Tissue
BCR-ABL1 Kinase Domain Mutation Analysis
BCR-ABL1, t(9;22) Translocation Qualitative by RT-PCR
BCR-ABL1, t(9;22) Translocation Quantitative Assay by RT-PCR
BRAF codon 600 Mutation Detection by Pyrosequencing
BRAF V600E Mutation with Reflex to MLH1 Promoter Methylation, Paraffinized Tissue
CEBPA Mutation Detection
CHOP Gene Rearrangement by FISH
Chromosome FISH, CLL Panel
Cytochrome P450 (CYP2C9)
Cytochrome P450 (CYP2D6)
Cytochrome P450 2C19 (CYP2C19) 9 Mutations
E2A-PBX1, t(1;19) Translocation by RT-PCR
EGFR by FISH
Ewing Sarcoma by RT-PCR
EWSR1 Break Apart Rearrangement by FISH
Familial Mutation, Targeted Sequencing
FKHR Gene Rearrangement by FISH
FLT3 Mutation Detection by PCR
Gastrointestinal Stromal Tumor Mutation
HER-2 Gene Amplification by Monoplex PCR
HER-2/neu by FISH (PathVysion HER-2)
HNPCC/Lynch Syndrome, (MLH1) Sequencing and Deletion/Duplication
HNPCC/Lynch Syndrome, (MSH2) Sequencing and Deletion/Duplication
HNPCC/Lynch Syndrome, (MSH6) Sequencing and Deletion/Duplication
HNPCC/Lynch Syndrome, (PMS2) Sequencing and Deletion/Duplication
HNPCC/Lynch Syndrome, Microsatellite Instability by PCR
IGH/BCL2 t(14;18) by FISH for Detection in Follicular Lymphoma
IGH/MYC, CEP8 t(8;14) by FISH for Detection in Burkitt Lymphoma
IgVH Mutation Analysis by Sequencing
inv(16) for AML(CBFB-MYH11) by RT-PCR
JAK2 Gene, V617 Mutation, Quantitation
JAK2 Gene, V617F Mutation, Qualitative
Juvenile Polyposis (SMAD4) Seqencing
Kaposi Sarcoma-Associated Herpesvirus/Human Herpesvirus 8
KIT (D816V) Mutation by PCR, Fluid
KIT (D816V) Mutation by PCR, Paraffin
KIT (D816V) Mutation by PCR, Tissue
KRAS Mutation Detection
KRAS Mutation Detection with BRAF Reflex
Methylenetetrahydrofolate Reductase (MTHFR) 2 Mutations
Microsatellite Instability/HNPCC by Immunohistochemical Stain
MLL-AF4, t(4;11) Translocation by RT-PCR
Multiple Endocrine Neoplasia Type 2 (MEN2), RET Gene Mutations by Sequencing
Multiple Endocrine Neoplasia, Type 2B (RET) 2 Mutations
Multiple Myeloma Panel by FISH
N-myc by FISH
NPM1 Mutation by PCR and Fragment Analysis, Fluid
NPM1 Mutation by PCR and Fragment Analysis, Paraffin
PAX-FKHR, Translocation by RT-PCR
PML-RARA, t(15;17) Translocation by RT-PCR
SYT Rearrangement by FISH
SYT-SSX, t(18;X) Translocations by RT-PCR
t(11;14) IgH-CCND1 Translocation by FISH
T-Cell Clonality Assessment by Restriction Fragment Southern Blot Hybridization, Fluid
T-Cell Clonality Assessment by Restriction Fragment Southern Blot Hybridization, Tissue
T-Cell Clonality Screening Assay by PCR, Fluid
T-Cell Clonality Screening Assay by PCR, Paraffin
T-Cell Clonality Screening Assay by PCR, Tissue
TEL-AML1, t(12;21) Translocation by RT-PCR
UDP glucuronosyltransferase 1A1 (UGT1A1) Genotyping
UroVysion™ FISH