The links allow you to take the module. You can also download the PowerPoint slides, full transcript, quiz questions, and answer key.
Laboratory Genomics
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This Laboratory Genomics course provides foundational knowledge and practical context for laboratory-based genomics work, including core concepts in molecular biology, laboratory techniques, and the interpretation of genomic data. The lectures and materials are designed to support hands-on laboratory training by introducing key principles, terminology, and methods used in modern genomics laboratories.
These materials were developed through a partnership between The Johns Hopkins University and the BioTechnical Institute of Maryland (BTI) to support BTI’s workforce training programs and to expand access to genomics education. The online lectures are intended to complement in-person laboratory instruction and provide learners with the background knowledge needed to engage more effectively in hands-on laboratory activities.
Cancer Module
This module introduces the genetic foundations of cancer and how genomic information is used to understand tumor development and guide clinical care. Learners explore how inherited and acquired genetic changes contribute to cancer risk, tumor growth, and treatment decisions. The module also highlights the role of genetic testing, family history, and targeted therapies in modern cancer medicine.
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Cardiology Module
This module introduces the genetic factors that contribute to inherited heart conditions. Learners explore how genetic variants can influence cardiac structure, rhythm, and metabolism, as well as how these conditions may run in families. The module also discusses the importance of genetic testing, family screening, and early detection in preventing serious cardiac events.
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Neonatal Module
This module focuses on the role of genetics in the care of newborns, including the purpose and process of newborn screening. Learners examine how early genetic and metabolic screening helps identify serious but treatable conditions shortly after birth. The module also introduces common follow-up testing, genetic consultations in neonatal care, and how genetic diagnoses can guide treatment and long-term monitoring.
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Pediatric Module
This module examines how genetic conditions present in childhood and how clinicians evaluate and diagnose these disorders. Learners explore the role of family history, physical examination, and genetic testing in identifying inherited conditions that affect growth, development, and health. The module highlights how genetic diagnoses can guide medical management and provide important information for families.
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Prenatal Module
This module explores how genetic information is used during pregnancy to assess potential health risks for a developing fetus. Learners review common prenatal screening and diagnostic approaches, including carrier screening, cell-free DNA screening, and diagnostic procedures. The module also discusses how genetic results help inform clinical decision-making, reproductive planning, and counseling for expectant families.
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Responsible Conduct of Research
This module introduces the ethical principles and professional standards that guide responsible scientific research. Learners examine topics such as human subjects protections, informed consent, data privacy, conflicts of interest, and research integrity. The module also explores the historical context that shaped modern research ethics and emphasizes the importance of transparency, collaboration, and accountability in scientific work.
