ThePrinciples in Genetics and Epigenetics (PIGE) class is designed for students who have a major interest in the aspects of experimental and human genetics and epigenetics as they relate to human disease, including Mendelian disorders, complex diseases and cancer. Students are required to have completed the core course (or equivalent). This class will provide in-depth instruction in four areas: 1) Experimental genetics, 2) Human genetics, 3) Epigenetics, 4) Applied bioinformatics. The class will be held two times a week for one and a half hours. Students are expected to actively participate in the course by initiating discussions, asking questions, and providing constructive comments, as well as completing weekly homework assignments based on the material covered in the lectures of the preceding week. Students will be evaluated by attendance, participation, bioinformatics workshop participation and completion of assigned exercises, and overall performance on the assigned homework. As a foundational course, this course is designed to introduce students to the basic principles in genetics and epigenetics and prepare the student to generate novel hypothesis-driven projects as part of their own research in the areas of genetics and epigenetics inside and outside of G&E laboratories. The course emphasizes active learning through a combination of didactic lectures, selected application lectures and a bioinformatics workshop. Auditing this course is permitted with Course Directors' approval.
This course is an introduction to the basic principles of human genetics and heredity. Students will investigate both classical Mendelian genetics and modern molecular genetics. Topics include the transmission of genes from one generation to the next, the molecular structure of genes, the regulation of gene expression, genes and cancer, genetic technology, genetically modified foods, gene therapy and population genetics. The course is designed for all students interested in human genetics, the application of genetic principles and genetic technology. (Prerequisites: BIOL133 or SCIN130)
This book covers some of the most novel genetic and genomic concepts in epidemiology, such as geospatial statistics and systems biology from a clinical point of view by explaining molecular applications with accessible human studies. Featuring a comprehensive table of contents, it includes chapters from genomics and epidemiology surveillance to transcriptomics and alternative splicing principles.
Across 17 well-organized chapters, this book meets attempt to explain easily to clinicians and students with basic principles of the genetics, genomics, molecular biology and its applications to epidemiology and public health. The text is distinct from other literature on the market because it covers useful genomic tools applied in epidemiology for clinicians who may not be experts in this branch of health science.
Nadia Alejandra Rivero Segura PhD is a Medical Researcher at Instituto Nacional de Geriatra in Mexico City. She holds a Bachelors in biology and was a postdoctoral fellow at Divisin de Neurosciencias-Instituto de Fisiologa Celular-UNAM. Co-editor of the above book with Springer, Clinical Genetics and Genomics of Aging, she is also the author of 15 scientific articles and 2 additional book chapters. She has performed a research stay at Instituto de Medicina Molecular Joan Lobo Antunes. Her research interests focus on neuroepigenetics of stroke, biomarkers of aging and mitochondrial dynamics in aging.
This course covers the principles of classical, molecular and population genetics in both model organisms and humans. Students explore inheritance, gene expression, population genetics and evolution, and genetic mutation and repair. The material emphasizes experimental evidence for genetic principles along with application of these principles to solve problems. Students perform investigative laboratory exercises in genetic mapping, recombinant DNA techniques, gene regulation, and bioinformatics.
Mitosis, meiosis, Mendelian genetics, chromosomes and inheritance, molecular basis of inheritance, genes to proteins, genetic models (viruses and bacteria), eukaryotic genomes, genetic basis of development and overview of genomes. Three lectures, 1 discussion section.
A Code of Ethics is a document which attempts to clarify and guide the conduct of a professional so that the goals and values of the profession might best be served. Download a PDF copy of the NSGC Code of Ethics.
If you require additional assistance interpreting the Code of Ethics in the context of a specific clinical case, research case, or professional issue, please consider submitting an Ethics Consult Request to the NSGC Ethics Advisory Group.
Genetic counselors are health professionals with specialized education, training, and experience in medical genetics and counseling. The National Society of Genetic Counselors (NSGC) is the leading voice, authority and advocate for the genetic counseling profession. Through this code of ethics, the NSGC affirms the ethical responsibilities of its members. NSGC members are expected to be aware of the ethical implications of their professional actions and work to uphold and adhere to the guidelines and principles set forth in this code.
A code of ethics is a document that attempts to clarify and guide the conduct of a professional so that the goals and values of the profession are best served. The NSGC Code of Ethics is based upon the distinct relationships genetic counselors have with 1) themselves, 2) their clients, 3) their colleagues, and 4) society. Each section of this code begins with an explanation of the relevant relationship, along with the key values and characteristics of that relationship. These values are drawn from the ethical principles of autonomy, beneficence, nonmaleficence and justice, and they include the professional principles of fidelity, veracity, integrity, dignity and accountability.
No set of guidelines can provide all the assistance needed in every situation, especially when different values appear to conflict. In certain areas, some ambiguity remains, allowing for the judgment of the genetic counselor(s) involved to determine how best to respond to difficult situations.
Genetic counselors value professionalism, competence, integrity, objectivity, veracity, dignity, accountability and self-respect in themselves as well as in each other. Therefore, genetic counselors work to:
The relationships of genetic counselors with society include interest and participation in activities that have the purpose of promoting the well-being of society and access to genetic services and health care. These relationships are based on the principles of veracity, objectivity and integrity. Therefore, genetic counselors, individually or through their professional organizations, work to:
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Gene expression involves transcription, translation and the turnover of mRNAs and proteins. The degree to which protein abundances scale with mRNA levels and the implications in cases where this dependency breaks down remain an intensely debated topic. Here we review recent mRNA-protein correlation studies in the light of the quantitative parameters of the gene expression pathway, contextual confounders and buffering mechanisms. Although protein and mRNA levels typically show reasonable correlation, we describe how transcriptomics and proteomics provide useful non-redundant readouts. Integrating both types of data can reveal exciting biology and is an essential step in refining our understanding of the principles of gene expression control.
Approach: A blended classroom approach combines online and classroom tools for teaching. We created four online learning modules to replace/supplement passive textbook reading with active learning activities to introduce and solidify genetics concepts prior to class time.
These modules were hosted on Blackboard. Each module consisted of a series of 3-5 short online video lectures. Each lecture is followed by a multiple choice formative assessment question associated with the information presented in the videos.
The students were given two attempts to answer each multiple choice question. If they answered incorrectly the first time, feedback was provided to guide them prior to their second attempt. The answer key for the formative assessment questions was also provided to the students the morning of class.
Finally, students were asked to attempt a more difficult genetics problem prior to class time. They were not expected to complete the problem. The problem was addressed during class time to promote a more active learning environment and to engage the students in higher levels of metacognitive understanding.
The results of the satisfaction survey revealed student perceptions about the modules. As you can see from these data, 91% of the students liked the modules even if they did not feel they were more effective than a traditional lecture. Regardless of their feelings about the modules, 68% of students found them more effective than traditional lectures. A second related question on the survey had similar results, which reveal that 78% of students believe that the online modules enhance their understanding of the concepts when compared to traditional lectures.
We also found that 58% of students found the pre-class problem helpful. When analyzing student comments, we found that some students found it useful to work through problems in class, but they felt like too much time was spent going through the problem during class and that it might be more beneficial to have additional group work.
Furthermore only 42% of students believed that the modules helped better prepare for the test when compared to in class lectures. However, 71% of students reported that they reviewed the modules when studying for the exam.
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