Code: | OPT177 | Acronym: | ONCOBAPLI |
Keywords | |
---|---|
Classification | Keyword |
OFICIAL | Medicine |
Active? | Yes |
Responsible unit: | Departamento de Patologia |
Course/CS Responsible: | Integrated Master in Medicine |
Acronym | No. of Students | Study Plan | Curricular Years | Credits UCN | Credits ECTS | Contact hours | Total Time |
---|---|---|---|---|---|---|---|
MIMED | 9 | Mestrado Integrado em Medicina- Plano oficial 2013 (Reforma Curricular) | 4 | - | 3 | 28 | 81 |
5 |
Tumor biology and genetics
Describe the mechanisms yielding to genetic variation, and be familiar with the various types of genetic variants.
Distinguish hereditary genetic anomalies from acquired genetic anomalies.
Discuss the advantages and limitations of different genetic laboratory methodologies for diagnostic testing.
Demonstrate how to interpret non-hotspot mutations using public databases and taking into account overall genomic aberrations and clonal evolution.
Be aware of ethical implications of incidental genetic findings.
Applied oncobiology
Describe main intracellular signaling pathways in solid tumors and molecular aberrations hampering this signaling.
Get detailed knowledge of immunological mechanisms and how these may be used to optimize therapeutic approaches.
Get a basic understanding of the principles underlying the design and analysis of clinical trials in oncology.
Understand the importance of predictive markers in molecular oncology.
Get familiar with the most frequent molecular aberrations in solid tumors and routinely used targeted therapies.
Bioinformatics
Communicate efficiently with bioinformaticians.
Describe a bioinformatics analysis pipeline to call mutations from NGS data.
Perform quality control at the run, read and variant levels.
Use off-the-shelf bioinformatics tools to annotate and support the interpretation of variants.
Consider hardware, security and privacy issues when managing omics data.
Understand how artificial intelligence contributes to and will further impact personalized oncology.
Molecular pathology
Understand the basics (procedures and rules) of an accredited clinical laboratory.
Gain knowledge about different types of specimens (e.g. tissue biopsy, cytology, resections).
Get familiar with all the steps that lead from samples collection to final molecular report generation along with all possible bottlenecks.
Have an overview about the currently used technological platforms in molecular diagnostics (comparison with the research setting).
Get familiar with the most common clinically relevant variants along with their interpretation and classification system.
Tumor biology and genetics
Describe the mechanisms yielding to genetic variation, and be familiar with the various types of genetic variants.
Distinguish hereditary genetic anomalies from acquired genetic anomalies.
Discuss the advantages and limitations of different genetic laboratory methodologies for diagnostic testing.
Demonstrate how to interpret non-hotspot mutations using public databases and taking into account overall genomic aberrations and clonal evolution.
Be aware of ethical implications of incidental genetic findings.
Applied oncobiology
Describe main intracellular signaling pathways in solid tumors and molecular aberrations hampering this signaling.
Get detailed knowledge of immunological mechanisms and how these may be used to optimize therapeutic approaches.
Get a basic understanding of the principles underlying the design and analysis of clinical trials in oncology.
Understand the importance of predictive markers in molecular oncology.
Get familiar with the most frequent molecular aberrations in solid tumors and routinely used targeted therapies.
Bioinformatics
Communicate efficiently with bioinformaticians.
Describe a bioinformatics analysis pipeline to call mutations from NGS data.
Perform quality control at the run, read and variant levels.
Use off-the-shelf bioinformatics tools to annotate and support the interpretation of variants.
Consider hardware, security and privacy issues when managing omics data.
Understand how artificial intelligence contributes to and will further impact personalized oncology.
Molecular pathology
Understand the basics (procedures and rules) of an accredited clinical laboratory.
Gain knowledge about different types of specimens (e.g. tissue biopsy, cytology, resections).
Get familiar with all the steps that lead from samples collection to final molecular report generation along with all possible bottlenecks.
Have an overview about the currently used technological platforms in molecular diagnostics (comparison with the research setting).
Get familiar with the most common clinically relevant variants along with their interpretation and classification system.
Tumor biology and genetics
Basic cytogenetics and molecular genetics
Hereditary vs. acquired genetics
Genetic recombination, DNA damage and repair
Solid tumors and hematological malignancies
Genetic predisposition to cancer
Diagnostic genetic testing
Clonal evolution & tumor heterogeneity
Applied oncobiology
Tumor Physiology
Tumor Immunology
Cancer Statistics and Epidemiology
Prognostic and Predictive Markers
Targeted Therapies in Clinical Oncology
Risks / probabilities for the interpretation of genetic results and counseling
Clinical Trials in Molecular Oncology
Bioinformatics
Data pre-processing
Read mapping
Variant calling
Quality control
Variant annotation
Hardware, security, privacy
Molecular pathology
Sample classification and preparation
Principles of nucleic acids extraction
Sequencing platforms and setup
Understanding gene panels
Internal / external Quality controls
Laboratory accreditation
Reporting genomic variants
Interpreting a molecular profile
Designation | Weight (%) |
---|---|
Participação presencial | 20,00 |
Exame | 80,00 |
Total: | 100,00 |
Designation | Time (hours) |
---|---|
Estudo autónomo | 53,00 |
Frequência das aulas | 28,00 |
Total: | 81,00 |
The final grade takes the form of a continuing component of class participation and a final exam with a written test with multiple-choice questions and short-answer questions. The assessment is expressed in the scale of 0 to 20 values. Approval requires a minimum grade of 10 and a frequency of at least 75% of the planned sessions.