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New Lab Tests
| Test Name | Methodology | Specimen | TAT | Lab |
|---|---|---|---|---|
| Precivity-ApoE™ | Mass Spectrometry | Whole Blood | 10 d | C2N Diagnostics |
| PrecivityAD2™ | Mass Spectrometry | Plasma | 10 d | C2N Diagnostics |
| PrecivityAD® | Mass Spectrometry | Whole Blood | 10 d | C2N Diagnostics |
| Pathlight™ Multi-cancer MRD test | NGS | Whole Blood, Tissue | 2-3 w | Saga Diagnostics |
| Cancerguard® Multi-Cancer Early Detection Test | Composite | Whole Blood | 10-14 d | Exact Sciences |
Precivity-ApoE™
Methodology:Mass Spectrometry
Specimen:Whole Blood
TAT:10 d
Lab:C2N Diagnostics
PrecivityAD2™
Methodology:Mass Spectrometry
Specimen:Plasma
TAT:10 d
Lab:C2N Diagnostics
PrecivityAD®
Methodology:Mass Spectrometry
Specimen:Whole Blood
TAT:10 d
Lab:C2N Diagnostics
Pathlight™ Multi-cancer MRD test
Methodology:NGS
Specimen:Whole Blood, Tissue
TAT:2-3 w
Lab:Saga Diagnostics
Cancerguard® Multi-Cancer Early Detection Test
Methodology:Composite
Specimen:Whole Blood
TAT:10-14 d
Lab:Exact Sciences
Featured Companion Diagnostics
| Test Name | Methodology | Specimen | TAT | Lab |
|---|---|---|---|---|
| xT CDx | NGS | Tissue, Whole Blood, Saliva | 10-14 d | Tempus AI |
| Vysis Chronic Lymphocytic Leukemia (CLL) Panel | Chromosomal / Cytogenetics | Whole Blood, Bone Marrow | 5 d | MPLN |
| PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome/Myeloproliferative Disease (MDS/MPD) | Chromosomal / Cytogenetics | Tumor Tissue | — | ARUP Laboratories |
| nAbCyte™ Anti‑AAVRh74var HB‑FE Assay (nAbCyte Assay) | Other | Serum | 7-10 d | Labcorp |
| MyChoice® CDx Myriad HRD Companion Diagnostic Test | NGS | Tissue | 14 d | Myriad Genetics |
xT CDx
Methodology:NGS
Specimen:Tissue, Whole Blood, Saliva
TAT:10-14 d
Lab:Tempus AI
Vysis Chronic Lymphocytic Leukemia (CLL) Panel
Methodology:Chromosomal / Cytogenetics
Specimen:Whole Blood, Bone Marrow
TAT:5 d
Lab:MPLN
PDGFRB FISH for Gleevec Eligibility in Myelodysplastic Syndrome/Myeloproliferative Disease (MDS/MPD)
Methodology:Chromosomal / Cytogenetics
Specimen:Tumor Tissue
TAT:—
Lab:ARUP Laboratories
nAbCyte™ Anti‑AAVRh74var HB‑FE Assay (nAbCyte Assay)
Methodology:Other
Specimen:Serum
TAT:7-10 d
Lab:Labcorp
MyChoice® CDx Myriad HRD Companion Diagnostic Test
Methodology:NGS
Specimen:Tissue
TAT:14 d
Lab:Myriad Genetics
Featured Sponsored Testing
| Program Name | Therapeutic Area(s) | Condition | Lab |
|---|---|---|---|
| Invitae Inherited Retinal Disorders Panel | Ophthalmology | Inherited Retinal Disease (IRD), Retinitis Pigmentosa (RP) | Invitae | Labcorp |
| X-ALD Newborn Screening Reflex Panel | Endocrinology, Metabolic | X-linked Adrenoleukodystrophy (X-ALD) | Prevention Genetics |
| Renasight™ Genetic Kidney Panel | Nephrology | Chronic Kidney Disease (CKD), APOL1-Mediated Kidney Disease (AMKD) | Natera |
| Color Hereditary Cancer Test | Oncology | Ovarian Cancer, Uterine/Endometrial Cancer | Color Health |
| NovoDETECT Primary Hyperoxaluria Panel | Nephrology | Primary Hyperoxaluria (PH) | Blueprint Genetics |
Invitae Inherited Retinal Disorders Panel
Therapeutic Area(s):Ophthalmology
Condition:Inherited Retinal Disease (IRD), Retinitis Pigmentosa (RP)
Lab:Invitae | Labcorp
X-ALD Newborn Screening Reflex Panel
Therapeutic Area(s):Endocrinology, Metabolic
Condition:X-linked Adrenoleukodystrophy (X-ALD)
Lab:Prevention Genetics
Renasight™ Genetic Kidney Panel
Therapeutic Area(s):Nephrology
Condition:Chronic Kidney Disease (CKD), APOL1-Mediated Kidney Disease (AMKD)
Lab:Natera
Color Hereditary Cancer Test
Therapeutic Area(s):Oncology
Condition:Ovarian Cancer, Uterine/Endometrial Cancer
Lab:Color Health
NovoDETECT Primary Hyperoxaluria Panel
Therapeutic Area(s):Nephrology
Condition:Primary Hyperoxaluria (PH)
Lab:Blueprint Genetics