- Abacavir Hypersensitivity Testing and Initial Patient Management Algorithm
- Acquired Neuropathy Diagnostic Algorithm
- Acute Leukemias of Ambiguous Lineage Testing Algorithm
- Acute Myeloid Leukemia Relapsed with Previous Remission Testing Algorithm
- Acute Myeloid Leukemia Testing Algorithm
- Acute Promyelocytic Leukemia Guideline to Diagnosis and Follow-up
- Acute Tickborne Disease Testing Algorithm
- Adulterant Survey Algorithm
- Aggressive B-cell Lymphoma Diagnostic Algorithm
- Alpha 1 Antitrypsin-A Comprehensive Testing Algorithm
- Amyloidosis Familial Test Algorithm
- Amyloidosis Laboratory Approach to the Diagnosis
- Anaplastic Large Cell Lymphoma Evaluation Algorithm
- Antinuclear Antibody Interpretive Algorithm
- Assessment for Dengue Virus Infection
- Assessment for Zika Virus Infection
- Autoimmune/Paraneoplastic Axonal Neuropathy Evaluation Algorithm
- Autoimmune/Paraneoplastic Dementia Evaluation Algorithm-Serum
- Autoimmune/Paraneoplastic Dementia Evaluation Algorithm-Spinal Fluid
- Autoimmune/Paraneoplastic Dysautonomia Evaluation Algorithm
- Autoimmune/Paraneoplastic Encephalopathy Evaluation Algorithm-Serum
- Autoimmune/Paraneoplastic Encephalopathy Evaluation Algorithm-Spinal Fluid
- Autoimmune/Paraneoplastic Epilepsy Evaluation Algorithm-Serum
- Autoimmune/Paraneoplastic Epilepsy Evaluation Algorithm-Spinal Fluid
- Autoimmune/Paraneoplastic Gastrointestinal Dysmotility Evaluation Algorithm
- Autoimmune/Paraneoplastic Movement Disorder Evaluation Algorithm – Serum
- Autoimmune/Paraneoplastic Movement Disorder Evaluation Algorithm-Spinal Fluid
- Autoimmune/Paraneoplastic Myelopathy Evaluation Algorithm-Serum
- Autoimmune/Paraneoplastic Myelopathy Evaluation Algorithm-Spinal Fluid
- Beckwith-Wiedemann and Russell-Silver Syndromes: Laboratory Approach to Diagnosis
- Bile Acid-Associated Tests Ordering Guide
- B-Lymphoblastic Leukemia/Lymphoma Genetic Testing Guidelines
- Bone Marrow Staging for Known or Suspected Malignant Lymphoma Algorithm
- Breast, Gynecological and Prostate Cancer Testing Algorithm
- Celiac Disease Comprehensive Cascade Test Algorithm
- Celiac Disease Diagnostic Testing Algorithm
- Celiac Disease Gluten-Free Cascade Test Algorithm
- Celiac Disease Routine Treatment Monitoring Algorithm
- Celiac Disease Serology Cascade Test Algorithm
- Central Nervous System Demyelinating Disease Diagnostic Algorithm
- Chimerism-Recipient Germline Testing Algorithm
- Chronic Hepatitis C Treatment and Monitoring Algorithm Direct Antiviral Agent DAA Combination
- Congenital Disorders of Glycosylation: Screening Algorithm
- Connective Tissue Disease Cascade
- Coronavirus Disease 2019 COVID19 Influenza and Respiratory Syncytial Virus Testing Algorithm
- Culture Referred for Identification and Susceptibility for Mycobacterium and Nocardia Algorithm
- Culture Referred for Identification Mycobacterium and Nocardia Algorithm
- CYP2D6 Comprehensive Cascade Testing Algorithm
- Cystic Fibrosis Molecular Diagnostic Testing Algorithm
- Galactosemia Testing Algorithm
- Ganglioside Antibody Panel Algorithm
- Gastric MALT Lymphoma Diagnostic Algorithm
- Gastric MALT Posttherapy Follow-up Algorithm
- Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency Diagnostic Algorithm
- Glucose-6-Phosphate Dehydrogenase (G6PD) Genotyping Interpretive Algorithm
- HBV Infection-Monitoring Before and After Liver Transplantation
- Helicobacter pylori Diagnostic Algorithm
- Hemophilia Carrier Testing Algorithm
- Hemophilia Testing Algorithm
- Hepatitis B Testing Algorithm for Screening, Diagnosis, and Management
- Hepatitis C Testing Algorithm for Screening and Diagnosis
- Hepatitis E Testing Algorithm for Diagnosis and Management
- Hereditary Hemochromatosis Algorithm
- Hereditary Hemolytic Anemia Evaluation Testing Algorithm
- Hereditary Peripheral Neuropathy Diagnostic Algorithm
- HIV Prenatal Testing Algorithm Including Followup of Reactive Rapid Serologic Test Results
- HIV Testing Algorithm (Fourth Generation Screening Assay), Including Follow-up of Reactive Rapid Serologic Test Results
- HIV Treatment Monitoring Algorithm
- Hyperoxaluria Diagnostic Algorithm
- Laboratory Testing for Infectious Causes of Diarrhea
- Lupus Anticoagulant Profile Testing Algorithm
- Lyme Neuroborreliosis Diagnostic Algorithm
- Lynch Syndrome Testing Algorithm
- Lysosomal Disorders Diagnostic Algorithm, Part 1
- Lysosomal Disorders Diagnostic Algorithm, Part 2
- Lysosomal Disorders Screen Interpretive Algorithm
- Malaria Laboratory Testing Algorithm
- Mast Cell Disorder Diagnostic Algorithm Bone Marrow
- Meningitis/Encephalitis Panel Algorithm
- Mosquito-borne Disease Laboratory Testing
- Multiple Myeloma Laboratory Screening
- Mycobacterium and Nocardia Culture Algorithm
- Myeloproliferative Neoplasm A Diagnostic Approach to Bone Marrow Evaluation
- Myeloproliferative Neoplasm A Diagnostic Approach to Peripheral Blood Evaluation
- Neuromuscular Myopathy Testing Algorithm
- Newborn Screen Follow-up for Acid Sphingomyelinase Deficiency
- Newborn Screen Follow-up for Decreased Citrulline
- Newborn Screen Follow-up for Decreased Free Carnitine (C0)
- Newborn Screen Follow-up for Elevated Arginine
- Newborn Screen Follow-up for Elevated C0; Elevated C0/(C16+C18)
- Newborn Screen Follow-up for Elevated C14:1 +/- Other Long-Chain Acylcarnitine
- Newborn Screen Follow-up for Elevated C16 +/- C18:1 Acylcarnitines
- Newborn Screen Follow-up for Elevated C16-OH +/- C18-OH
- Newborn Screen Follow-up for Elevated C4 and C5 Acylcarnitine +/- Other Elevated Acylcarnitines
- Newborn Screen Follow-up for Elevated C4-OH Acylcarnitine
- Newborn Screen Follow-up for Elevated C5-DC
- Newborn Screen Follow-up for Elevated C5-OH
- Newborn Screen Follow-up for Elevated C8 Acylcarnitine with Lesser Elevations of C6 and C10 Acylcarnitines
- Newborn Screen Follow-up for Elevated Citrulline
- Newborn Screen Follow-up for Elevated Leucine
- Newborn Screen Follow-up for Elevated Methionine
- Newborn Screen Follow-up for Elevated Phenylalanine
- Newborn Screen Follow-up for Elevated Tyrosine, Normal Succinylacetone
- Newborn Screen Follow-up for Elevated/Normal Tyrosine, Elevated Succinylacetone
- Newborn Screen Follow-up for Gaucher Disease
- Newborn Screen Followup for Glucose6Phosphate Dehydrogenase G6PD Deficiency
- Newborn Screen Followup for Guanidinoacetate Methyltransferase Deficiency
- Newborn Screen Follow-up for Isolated Elevation of C3
- Newborn Screen Follow-up for Isolated Elevation of C3-DC
- Newborn Screen Follow-up for Krabbe Disease Galactocerebrosidase
- Newborn Screen Follow-up for Krabbe Disease Galactocerebrosidase and Psychosine
- Newborn Screen Follow-up for Mucopolysaccharidosis Type I
- Newborn Screen Follow-up for Mucopolysaccharidosis Type II
- Newborn Screen Follow-up for Pompe Disease
- Newborn Screen Followup for Severe Combined Immunodeficiency Syndrome SCID
- Newborn Screen Follow-up for X-Linked Adrenoleukodystrophy
- Parasitic Investigation of Stool Specimens Algorithm
- Pathology Consultation Ordering Algorithm
- Pediatric Autoimmune Central Nervous System Demyelinating Disease Diagnostic Algorithm
- Pediatric Autoimmune Encephalopathy/Central Nervous System Disorders Evaluation Algorithm-Serum
- Pediatric Autoimmune Encephalopathy/Central Nervous System Disorders Evaluation Algorithm-Spinal Fluid
- Platelet Antibody Testing Algorithm
- Porphyria Acute Testing Algorithm
- Porphyria Cutaneous Testing Algorithm
- Postmortem Screening Algorithm for Fatty Acid Oxidation Disorders and Organic Acidurias
- Prader-Willi and Angelman Syndromes Laboratory Approach to Postnatal Diagnosis