Technical Bulletins
Written by ARUP's medical directors and added to this list on a bimonthly basis, technical bulletins provide interpretive data regarding newly available tests, including methodologies and clinical significance.
Available Technical Bulletins by Topic
#
- 1,5-Anhydroglucitol (GlycoMark®)
- 16S rDNA Organism Identification
- 17-Hydroxyprogesterone Analysis in Serum by LC-MS/MS
- 1p and 19q by FISH
- 21-Hydroxylase Antibody
- 25-Hydroxyvitamin D2 and D3 in Serum by LC-MSMS
- 5-Fluorouracil Sensitivity (DPYD, TYMS, and MTHFR), 8 Mutations
A
- Acetylcholine Receptor Antibody Testing
- Achondroplasia Genotyping
- Acute Myeloid Leukemia (AML) Panel by FISH
- Adiponectin
- Adrenal Steroids Panel
- AFP-L3% in Serum (Includes Total Alpha-Fetoprotein)
- Aggressive Lymphoma Panel by FISH
- Alpha-1-Antitrypsin Deficiency, Genotyping
- Alpha Thalassemia HBA1 and HBA2 Common Gene Deletions or Sequencing
- Alport Syndrome, Adult Type (COL4A5) 3 Mutations
- Alport Syndrome, X-Linked (COL4A5) Sequencing
- AML with MDS or Therapy-Related MDS Panel by FISH
- Androstenedione and Dehydroepiandrosterone in Serum by LC-MS/MS
- Angelman Syndrome Methylation
- Ankylosing Spondylitis (HLA-B27) Genotyping
- Anti-Actin IgA in Celiac Disease
- Anti-MAG and Anti-SGPG, IgM
- Antiphospholipid Syndrome (APS) Testing
- Apolipoprotein B (APOB) 2 Mutations
- Apolipoprotein E (APOE) 2 Mutations, Cardiovascular Risk
- Arsenic Fractionation
- Ashkenazi Jewish Diseases
B
- Bartonella DNA Detection by PCR
- BCR/ABL1 Kinase Domain Mutation Analysis
- BCR/ABL, t(9;22) Translocastion Assays
- Beta-2-Adrenergic Receptor (ADRB2) Haplotyping
- Beta Globin (HBB) HbS, HbC, and HbE Mutations
- Beta Globin (HBB) Sequencing
- Bile Acids, Fractionated and Total
- Biotinidase Deficiency (BTD)
- Blood Group Microarray, Nine Blood Groups
- Bordetella pertussis Antibodies, IgA, IgG & IgM
- BRAF V600E Mutation and MLH1 Promoter Methylation Detection in Colon Cancer
- BRAF V600E Mutation in Thyroid by PCR, Paraffin
C
- Calprotectin (CALPRO), Fecal
- Candida albicans Antibody Detection Panel by ELISA
- Carbohydrate-Deficient Transferrin (CDT) for Alcohol Use
- Chimerism by STR Genotyping
- CHOP Gene Rearrangement by FISH
- Chronic Lymphocytic Leukemia
- Chronic Lymphocytic Leukemia Follow Up Phenotyping by Flow Cytometry
- Circulating Tumor Cell (CTC) Count
- Clostridium difficile toxin B gene (tcdB) by PCR
- Creatine Deficiency Syndromes
- Cross-Linked C-Telopeptides in Serum
- Cryoglobulin, Qualitative with Reflex to IFE Typing and Quantitative IgA, IgG, and IgM
- Cystic Fibrosis Cis-Trans (CFTR)R117H & 5T Mutations
- Cystic Fibrosis (CFTR) 3199del6 Mutation
- Cystic Fibrosis (CFTR) 32 Mutations
- Cystic Fibrosis (CFTR) 32 Mutations, Atypical
- Cystic Fibrosis (CFTR) 32 Mutations with Reflex to Sequencing and Deletion/Duplication
- Cytochrome P450 2C9 (CYP2C9) 2 Mutations
- Cytochrome P450 2C19 (CYP2C19) 7 Mutations
- Cytochrome P450 2D6 (CYP2D6)14 Mutations & Gene Duplication
- Cytochrome P450 2D6 Genotyping to Predict Metabolic Activation of Tamoxifen
- Cytokeratin 19 Fragment (CYFRA 21-1) Serum
D
- Dengue Fever Virus Antibodies, IgG and IgM
- Des-γ-Carboxy Prothrombin (DCP) in Serum
- Desmoglein 1 and Desmoglein 3 IgG Antibodies in Serum
- Detection of Amphiphysin IgG Antibodies
- Disaccharidase, Tissue
- Drugs of Abuse, Identification and Quantification in Meconium
- Drugs of Abuse, Opiates and Related Drugs
E
- E2A-PBX1 t(1 19) Translocation by RT-PCR and Fluorescence Monitoring
- EGFR Mutations by Capillary Electrophoresis
- Eosinophil Granule Major Basic Protein in Tissues
- Eosinophilia Panel by FISH
- Epithelial Skin Antibody
- Everolimus (Zortress®)
- Ewing Sarcoma Family of Tumors
- Estradiol and Estrone in Serum by LC-MS-MS
F
- F-Actin (Smooth Muscle) IgG by Enzyme Immunoassay
- Factor II (F2) G20210A Mutation
- Factor V Leiden (F5) R506Q Mutation
- Factor V R2 A4070G Mutation
- Familial Mediterranean Fever (MEFV) Sequencing
- FG Syndrome (MED12) R961W Mutation
- FKHR by FISH on Formalin-Fixed, Paraffin-Embedded Tissue
- FOXL2 Mutation Detection by Pyrosequencing
- Fragile X (FMR1) Mutation
- Free Copper (Direct) in Serum Ultrafiltrate
- Free Cortisol and Cortisone in Urine
- Freeman-Sheldon Syndrome (MYH3) Sequencing, Exon 17
G
- Galactosemia Panel
- Galactosemia Sequencing
- Gastrointestinal Stromal Tumors (GISTS), Mutation Detection
- Genomic (CGH) Microarray Analysis
- Gliadin Peptide Antibodies, IgA & IgG
- Glaucoma (Primary Congenital), CYP1B1 Sequencing
- Glucose-6-Phosphate Dehydrogenase (G6PD) DNA Mutation
- Glutarylcarnitine Quantitation for Glutaric Acidemia Type I
H
- Haptoglobin (HP) Genotyping
- Hearing Loss Panel, Nonsyndromic (GJB2) Sequencing, (GJB6) 2 Deletions and Mitochondrial 2 Mutations
- Helicobacter pylori Breath Test
- Hemochromatosis (HFE) 3 Mutations
- Hemophilia A (F8) Inversion, Sequencing, and Deletion/ Duplication
- Hemophilia B (F9) Sequencing
- Hepatitis C Virus (HCV) RNA Quantitative Real-time PCR
- HER2 Gene Amplification in Breast Cancer by Monoplex PCR
- HER2 by FISH
- HER2 CISH
- HER-2/neu, Serum
- Hereditary Hemorrhagic Telangiectasia (ENG and ACVRL1) Sequencing
- HLA-B*5701 Genotyping, Abacavir Sensitivity
- HNPCC/ Lynch Syndrome, Microsatellite Instability by PCR
- Human Immunodeficiency Virus 1 RNA Quantitative Real-time PCR
- Human Leptin
- Human Metapneumovirus by Real-Time RT-PCR
- Human Metapneumovirus (hMPV) Detection by DFA
- Human Papillomavirus (HPV) Genotyping
- Huntington Disease (HD)
- Hyaluronic Acid
- Hypertrophic Cardiomyopathy Resequencing Array
- Hypochondroplasia (FGFR3) 2 Mutations
I
- IBD Prognostic Panel
- Idiopathic and Hereditary Pancreatitis
- IgA Pemphigus IgA Epithelial Cell Surface Antibodies
- IGH/BCL2 Translocation by FISH
- IgH-CCND1 by FISH on Formalin-Fixed, Paraffin-Embedded Tissue
- Ig VH Gene Analysis for Chronic Lymphocytic Leukemia Prognosis
- Immunosuppressants by Tandem Mass Spectrometry
- Inflammatory Bowel Disease
- Inhibin B
- Interleukin-1-Receptor-Associated Kinase-4 (IRAK-4)
- Intraepidermal Nerve Fiber Density Analysis
- inv(16) for AML(CBFB-MYH11) by RT-PCR
J
- JAK2 (V617F) Mutation by PCR
- JAK2 c.1849G-T (V617F) Mutation Quantification by Real-Time PCR
- Juvenile Polyposis (SMAD4) Sequencing and Deletion/Duplication
K
- Kaposi Sarcoma-Associated Herpesvirus-Human Herpesvirus 8
- Kell Antigen Genotyping (KEL1-KEL2)
- KIT (D816V) Mutation by PCR
- KIT Exon 8 and 17 Mutations in Acute Myeloid Leukemia
- KIT Mutations Analysis in Melanoma
- KRAS Mutation Detection in Colorectal Cancer
L
- Legius Syndrome (SPRED1) Sequencing & (NF1) Sequencing Exon 22 (Exon 17)
- Lipoprotein-Associated Phospholipase A2 (PLACTM)
- Loeys-Dietz Syndrome (TGFBR1 and TGFBR2) Sequencing and Deletion Duplication
- Lyme Disease
- Lymphocytic Choriomeningitis (LCM) Virus by IFA
- Lynch Syndrome
M
- Macular Degeneration, Age-Related
- Malaria Antibodies, IgG by ELISA
- Maternal Screening, Sequential
- Maternal Serum Screen, First Trimester
- Maternal Serum Screening, Integrated Test
- Maternal Serum Screening, Quadruple
- Medium Chain Acyl-CoA Dehydrogenase (MCAD)
- Methotrexate Sensitivity (MTHFR) 2 Mutations
- Methylenetetrahydrofolate Reductase (MTHFR) Mutation Detection
- Microarray, Genomic, Fetal
- Mitochondrial Genome Mutation Scanning
- Mucopolysaccharides, Screen and Quantitation
- Multiple Myeloma (MM) by FISH
- Multiple Endocrine Neoplasia Type 2 (MEN 2)
- Mutation Detection in Gastrointestinal Stromal Tumors (GISTs)
- Mycobacteria Identification and Susceptibility Testing
- Mycobacterium Tuberculosis Complex Speciation
- Mycobacterium Tuberculosis IgG Antibody Detection by ELISA
- Myelodysplastic Syndrome (MDS) Panel by FISH
- Myeloproliferative Disorder (MPD) Panel by FISH
N
- Neoplastic Mature T-Cell Evaluation by Flow Cytometry
- Neopterin
- Neurofibromatosis Type 1 (NF1) Deletion/Duplication
- Neuronal-Specific Enolase (NSE) in Cerebrospinal
- Nicotine and Related Compounds in Urine and SerumPlasma
- NPM1 Mutations in Acute Myelogenous Leukemia
- NMR LipoProfile Test
- Noonan Syndrome (PTPN11) Sequencing
- Norovirus by RT-PCR
- Novel Screening Assay for Celiac Disease and Dermatitis Herpetiformis
O
P
- PATHWAY® HER-2/neu (4B5)
- PAX-FKHR Translocations by RT-PCR
- PCA3—Prostate Cancer Biomarker
- Pemphigus Panel
- Platelet Antigen (HPA1, HPA2, HPA3, HPA4, HPA5, HPA6, and HPA15) Genotyping
- PML-RARa t(15;17) Translocation by RT-PCR
- Prader-Willi Syndrome
- Primary Carnitine Deficiency (SLC22A5) Full Gene Sequencing
- Procalcitonin (PCT)
- Procollagen Type 1 N-Terminal Propeptide
- Prolactin Macroadenoma
- PTEN-Related Disorders, Sequencing and Deletion/Duplication
Q
- QuantiFERON®-TB Gold In-Tube Method
- QuantiFERON®-TB Gold In-Tubeand Mycobacterium tuberculosis Antibody, IgG by ELISA
R
- Rabies IgG Antibody Detection by ELISA
- RASA1 Sequencing
- Recurrent Genetic Abnormalities in Adult B-Cell Acute Lymphoblastic
- Recurrent Genetic Abnormalities in Pediatric B-Cell Acute Lymphoblastic
- Rett Syndrome (MECP2) Sequencing and Deletion/ Duplication
- RhD Antigen (RHD) Genotyping
- RhEe and RhCc Antigen (RHCE) Genotyping
S
- S-100B Protein, Serum (for Acquired Brain Injury)
- S-100B Protein, Serum (for Melanoma)
- Salivary Cortisol
- SMAD4 (MADH4) Full Gene Sequencing
- Schistosoma IgG Antibody Detection by ELISA
- Soluble CD30, Fluorescent Immunoassay
- Soluble Mesothelin-Related Peptides (MESOMARK®)
- Specimen Identity Testing
- Squamous Cell Carcinoma Antigen
- Strongyloides Antibody Detection by ELISA
- SYT-SSX t(X;18) Translocations by RT-PCR
T
- T-Cell Clonality by Flow Cytometry Analysis of TCR V-Beta
- T. Cruzi (Chagas' Disease) IgG Antibody Detection by Rapid Test
- Thanatophoric Dysplasia, Types 1 & 2 (FGFR3) 13 Mutations
- Thiopurine Methyltransferase, Red Blood Cell
- Toll-Like Receptor Function (TLR) Assay
- Total Coenzyme Q10 by HPLC, Plasma or Serum
U
- UGT1A1 (TA) n Polymorphisms and Expression of Uridine
- Urine Supersaturation Profile
- UroVysion(TM) FISH
V
- Very Long-Chain Acyl-CoA Dehydrogenase / VLCAD (ACADVL) Sequencing
- Visceral Leishmaniasis Antibody Detection by Rapid Test
- Vitamin D, 1,25-Dihydroxy and Vitamin D
- Vitamin B1 in Whole Blood by HPLC
- Vysis® LSI® MYC Dual Color, Break Apart Rearrangement Probe
W
X
Y
Z
Related information
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