This test uses targeted next-generation sequencing to evaluate for somatic mutations within the EGFR, BRAF, KRAS, HRAS, NRAS, ALK, ERBB2, and MET genes. Next-generation sequencing is also used to identify rearrangements (fusions) involving ALK, ROS1, RET, and NTRK1.
When this test is ordered, slide review will always be performed at an additional charge.
Third Generation LH assay
Ultrasensitive LH assay
Lyme CNS Infection IgG Screen
Reflex test: Lyme CNS Infection, IgG
Blastogenesis Antigens Immune Competence Lymphocyte Blastogenesis Antigen Lymphocyte Phytohemagglutiin Lymphocyte Transformation
If insufficient peripheral blood mononuclear cells (PBMCs) are isolated from the patient's sample due to low WBC counts or specimen volume received, selected dilutions or stimulants may not be tested at the discretion of the laboratory to ensure the most reliable results. Testing with 1 stimulant will always be performed. When adequate specimen is available for both stimulants to be tested, an additional test ID will be reflexed and billed separately.
Alpha-Fucosidosis Alpha-Galactosidase Deficiency Alpha-Mannosidosis Alpha-N-Acetylgalactosaminidase Deficiency Arylsulfatase A Deficiency Arylsulfatase B Deficiency Aspartylglucosaminuria Aspartylglycosaminuria Beta-Galactosidase Deficiency Beta-Glucuronidase Deficiency Ceramide Hexosides Ceramide Trihexosidase Ceramide Trihexosidase Deficiency Chondroitin-6-sulfate Chondroitin-6 sulfate Dermatan Sulfate Diffuse Angiokeratoma Fabry Disease Fabry's Disease GAGS (Glycosaminoglycans) Galactose-6-Sulfatase Deficiency Galactosialidosis GB3 GL3 Globotriaosylceramide Glycosaminoglycans (GAGS) GM1 gangliosidosis GM2 gangliosidosis Heparan Sulfate Hunter Syndrome Hurler Syndrome Hurler-Scheie Syndrome I-Cell Disease Iduronate Sulfatase Deficiency Iduronidase Deficiency Keratan Sulfate LSD Lysosomal Storage Lysosomal Storage Disease Maroteaux Lamy Syndrome Maroteaux-Lamy Syndrome Metachromatic Leukodystrophy Morquio A Morquio B MPS I MPS II MPS III MPS IVA MPS IVB MPS VI MPS VII Mucolipidosis II Mucolipidosis III Mucopolysaccharides Mucopolysaccharidosis Multiple Sulfatase Deficiency Oligosaccharides Oligosaccharidosis Pompe Disease Pseudo-Hurler Polydystrophy Sandhoff Disease Sanfilippo Syndrome Scheie Syndrome Schindler Disease Sialidosis Sly Syndrome Sphingolipids Sulfatides
This test contains a combined analysis of ceramide trihexosides, mucopolysaccharides, oligosaccharides, and sulfatides. This combined analysis of these disease-specific markers allows for the identification of disorders that may not be picked up using any of the single tests alone.