Practise Specialist in Molecular Biology (SMB) with a short sample and answer explanations. These are independent learning materials, not official exam questions or a pass prediction.
Exam outline and official sources
American Society for Clinical Pathology Board of Certification (ASCP BOC) · Specialist in Molecular Biology—SMB(ASCP) and SMB(ASCPi), Examination Content Guideline, revised September 25, 2025. The document states a revision date but no separate effective date. The workbook label SMB maps to the official Specialist in Molecular Biology credential; the guideline covers both ASCP and ASCPi pathways.
This original 20-question sample covers selected topics across the outline. It does not reproduce official exam questions or cover every tested topic.
- Specialist in Molecular Biology—SMB(ASCP) and SMB(ASCPi): Examination Content Guideline
- NHGRI: Ribonucleic Acid Fact Sheet
- NHGRI: Autosomal Recessive Disorder
- Thermo Fisher Scientific: TaqMan vs. SYBR Chemistry for Real-Time PCR
- Applied Biosystems: Amplification Efficiency
- Thermo Fisher Scientific: What Is Sanger Sequencing?
- MRC Holland: Is It Possible to Detect SNVs with MLPA and digitalMLPA?
- Illumina: Sequencing Quality Scores
- Illumina DRAGEN: QC Metrics and Coverage/Callability Reports
- QIAGEN CLC Genomics Workbench: Detecting DNA Methylation
- CDC: Good Laboratory Practices for Molecular Genetic Testing for Heritable Diseases and Conditions
- CMS: CLIA Verification of Performance Specifications
- CMS: Proficiency Testing and PT Referral
- NIST: Coefficient of Variation
- FDA: Statistical Guidance on Reporting Results from Studies Evaluating Diagnostic Tests
- FDA: Establishing Performance Characteristics of Devices for Detection or Differentiation of Influenza Viruses
- FDA: Commercially Distributed Analyte Specific Reagents—Frequently Asked Questions
- Association for Molecular Pathology: Molecular Diagnostic Assay Validation White Paper
- European LeukemiaNet: Laboratory Recommendations for Diagnosis and Management of Chronic Myeloid Leukemia
- ARUP Laboratories: Angelman Syndrome and Prader-Willi Syndrome by Methylation-Specific MLPA
- CDC: Clinical Testing and Diagnosis for C. diff Infection
- ARUP Laboratories: Chimerism Testing by Short Tandem Repeat Genotyping
- CPIC Guideline for CYP2C19 Genotype and Clopidogrel Therapy: 2022 Update
- National Cancer Institute: BRCA Gene Changes—Cancer Risk and Genetic Testing
- ARUP Laboratories: FMR1 Premutation Example Report
- NMDP: HLA Reporting Background
- ASCP BOC: Earn a Credential
- NHGRI: Talking Glossary of Genomic and Genetic Terms
- New England Biolabs: Isothermal Amplification and Strand Displacement
- Hologic: Aptima HPV 16 18/45 Genotype Assay—Instructions for Use, AW-26281-001 Rev. 001
- Thermo Fisher Scientific: QuantiGene Assays for Analysis of Gene Expression Utilizing Branched DNA Technology
- Thermo Scientific: Shake 'n Stack Hybridization Oven Operating and Maintenance Manual
- NHGRI: Fluorescence In Situ Hybridization Fact Sheet
- CMS: CLIA Assessing Personnel Competency
- OSHA: Laboratories—Overview
- MedlinePlus Genetics: HBA2 Gene
- MedlinePlus Genetics: HBB Gene
- MedlinePlus Genetics: F5 Gene
- MedlinePlus Genetics: F2 Gene
- MedlinePlus Genetics: MTHFR Gene
- NHGRI: Researchers Examine Disease-Causing Mutations in Mitochondrial Genomes
Specialist in Molecular Biology (SMB)
Start with 20 free questions, then review the explanations and any topics you missed.
Validated genomic sequencing and dosage analysis demonstrate that exons 1, 2, and 3 are intact on both alleles of a gene. RNA analysis identifies a transcript joining exon 1 directly to exon 3, while another transcript contains all three exons. Which process most directly explains this difference?
Specialist in Molecular Biology (SMB)
Flashcards
Molecular Science
Basic Molecular Theory—Translation
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