| Literature DB >> 31246944 |
Angela C Davies1, Diane Harris2, Amanda Banks-Gatenby2, Andy Brass1.
Abstract
We have now reached the genomics era within medicine; genomics is being used to personalise treatment, make diagnoses, prognoses, and predict adverse outcomes resulting from treatment with certain drugs. Genomic data is now abundant in healthcare, and the newly created profession of clinical bioinformaticians are responsible for its analysis. In the United Kingdom, clinical bioinformaticians are trained within a 3-year programme, integrating a work-based placement with a part-time Master's degree. As this profession is still developing, trainees can feel isolated from their peers whom are located in other hospitals and can find it difficult to gain the mentorship that they require to complete their training. Building strong networks or communities of practice (CoPs) and allowing sharing of knowledge and experiences is one solution to addressing this isolation. Within the Master's delivered at the University of Manchester, we have integrated group-centred problem-based learning (PBL) using real clinical case studies worked on during each course unit. This approach is combined with a flipped style of teaching providing access to online content in our Virtual Learning Environment before the course. The face-to-face teaching is used to focus on the application of the students' knowledge to clinical case studies. In this study, we conducted semistructured interviews with 8 students, spanning 3 cohorts of students. We evaluated the effectiveness of this style of teaching and whether it had contributed to the formation of CoPs between our students. Our findings demonstrated that this style of teaching was preferred by our students to a more traditional lecture-based format and that the problem-based learning approach enabled the formation of CoPs within these cohorts. These CoPs are valuable in the development of this new profession and assist with the production of new guidelines and policies that are helping to professionalise this new group of healthcare scientists.Entities:
Mesh:
Year: 2019 PMID: 31246944 PMCID: PMC6597031 DOI: 10.1371/journal.pcbi.1006746
Source DB: PubMed Journal: PLoS Comput Biol ISSN: 1553-734X Impact factor: 4.475
Course structure, including unit titles (1 credit is equivalent to 10 notional hours of learning).
| Year | Unit Title | Credits |
|---|---|---|
| 1 | Professional Practice and Introduction to Healthcare Sciences | 15 |
| 1 | Clinical Bioinformatics | 10 |
| 1 | Generic Content (Human Physiology) | 5 |
| 1 | Clinical Bioinformatics 2 | 30 |
| 1 | Programming | 15 |
| 1 | Applied Clinical Bioinformatics: Applied Next Generation Sequencing | 10 |
| 2 | Advanced Clinical Bioinformatics | 15 |
| 2 | Research Project Part 1 | 30 |
| 2 | Research Methods | 0 |
| 3 | Applied Clinical Bioinformatics: Whole Systems Molecular Medicine | 10 |
| 3 | Applied Clinical Bioinformatics: Advanced IT | 10 |
| 3 | Research Project Part 2 | 30 |
| Total | 180 |
Abbreviations: IT, Information Technology.
Example structure of morning traditional style lectures in the introduction to clinical bioinformatics module.
| Day | Morning (3 hours) | Example Intended Learning Outcomes |
|---|---|---|
| 1 | Introductory lectures on molecular biology, genetics, genomics, and sequencing. | Describe the structure of DNA and the functions of coding and noncoding DNA. |
| 2 | Introductory lectures on bioinformatics, including, primary sequence databases, genome browsers, creating alignments, and assessing homology, genotype, and phenotype ontologies. | Describe appropriate bioinformatics databases capturing information on DNA, RNA, and protein sequences. |
| 3 | Introduction of clinical bioinformatics databases that are useful for assessing the pathogenicity of a genetic variant. | Describe secondary databases in bioinformatics and their use in generating metadata on gene function. |
| 4 | Clinical case studies presented by a clinical scientist, using current best practice guidelines to assess all sources of evidence and assign the pathogenicity of a variant. | Describe the biological background to diagnostic genetic testing and clinical genetics and the role of bioinformatics. Describe the partnership of clinical bioinformatics and genetics to other clinical specialisms in the investigation and management of genetic disorders and the contribution to safe and effective patient care. |
| 5 | Task 5: Prepare a 15-minute presentation to be given by the group on the analysis on their variant, including a clinical report outlining their assessment of the variant’s pathogenicity. | Apply the knowledge of clinical bioinformatics to address specific clinical problems. |
Example structure of afternoon group PBL-based activity within the introduction to clinical bioinformatics module.
| Day | Afternoon Group Activity (3 hours) | Intended Learning Outcomes | Formative Feedback |
|---|---|---|---|
| 1 | Investigation of a genetic variant taken from a real clinical genetics case study. | Discuss and justify the importance of standards, best practice guidelines, and SOPs and how they are developed, improved, and applied to clinical bioinformatics. | To undertake this task, students are asked to create a SOP; feedback is provided on this SOP and on the information that they have retrieved. |
| 2 | Task 2: Locate the gene, correct transcript, and variant. Download homologous sequences, create a sequence alignment, and assess conservation at the position of the variant. | Perform analysis on DNA data and protein sequence data to infer function. | To undertake this task, students are asked to create a SOP; feedback is provided on this SOP and on the information that they have retrieved. |
| 3 | Task 3: Analyse clinical bioinformatics databases for presence of the variant and use this evidence to assess the pathogenicity of the variant. | Select and apply appropriate bioinformatic tools and resources from a core subset to typical diagnostic laboratory cases, contextualised to the scope and practice of a clinical genetics’ laboratory. | To undertake this task, students are asked to add to their SOP from day 2; feedback is provided on this SOP and on the information that they have retrieved. |
| 4 | Task 4: Bring all lines of evidence together to assess the pathogenicity of the clinical variant. | Communicate complex ideas and arguments in a clear, concise, and effective manner. | Facilitators on hand to field questions from their groups. |
| 5 | Task 6: Deliver presentation as a group and answer questions. | Work effectively as an individual or part of a team. | Clinical scientist to ask questions and provide formative feedback on the students’ analyses. |
Abbreviations: PBL, problem-based learning; SOP, Standard Operating Procedure.
Fig 1Flipped model of teaching used within the course.
Breakdown of study time for the 10-credit introduction to clinical bioinformatics unit.
| Learning Component | Hours | Assessment: Percentage of Unit Mark |
|---|---|---|
| Online resources, reading, and tutorials | 35 | - |
| Face-to-face lectures | 12 | - |
| PBL (groups) | 18 | 30% |
| Individual assignment | 25 | 70% |
Abbreviation: PBL, problem-based learning.
Interview schedule.
| Starting question | Elements to draw out with sub questions |
|---|---|
| 1. Experiences of professional practice before starting the course | • Role |
| 2. Student view of the structure and content of the course so far | How do they now perceive: |
| 3. What aspects of the course so far have stood out | • Positively and negatively |
| 4. Relationship with fellow students during the very first taught section of the course | • Level of contact |
| 5. Relationship with fellow students now | • Both within course and in practice |
| 6. Any contact with fellow students between taught sessions | • How often? |
| 7. Any contact with students in other cohorts | • Do they work together either in course or in practice/ locally or virtually? |
| 8. Student view of which aspects of the course contributed to above (relationship and contact with other students) | Returning to earlier answers, what aspect of the course (as per their perception Q2; content, teachers, activities, etc.) influenced: |
| 9. Predict how course has/will influence future practice | • What roles and ways of working envisaged |
Ten emergent themes identified from interview transcripts.
| Theme | Additional Comments |
|---|---|
| Communities of practice | shared repertoire of new practice in bioinformatics. |
| New career | specialism has no history and so depends on negotiation with potential employers. |
| Isolation in practice | students talk about being ‘the only one’ in the hospital. |
| Accountability | the practice is not established. |
| Teaching/learning | group work, traditional lectures, flipped teaching. |
| Ownership of the course | student feedback has influenced subsequent presentations of the course. |
| Joint enterprise | nothing decided by the institutions/professional body so ‘joint enterprise’ is the decision, responsibility of the group. |
| Talk about group and dynamics | not during studies but social aspects and holidays. |