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Genetics and genomics play a vital role in health and disease. Genetics refers to the science of variation and biological inheritance. The fundamental principles are adopted by molecular genetics, genomics, cytogenetics, 'Mendelian' genetics, population genetics, epigenetics, and quantitative genetics.
On the other hand, genomics is a new discipline developed by geneticists and genome scientists for generating large data sets through high-throughput RNA, DNA, and protein techniques, and the requirement for determining the control of biological roles via informatics analysis of huge data sets produced.
Students pursuing the genetics and genomics course have to submit heaps of assessments with strict deadlines to complete the course. These assessments require DNA analysis and knowledge of various methodologies for its expression. Students must also hold a strong grip on conceptual understanding, including universal principles, issues, and potentials associated with DNA-based life.
Students generally get stuck while solving the tasks as they fail to identify and critically evaluate genetic issues. Are you in a similar plight? If yes, don’t be worried anymore. You have landed at the right place! Our proficient online educators are available 24*7 to provide you with the best approach to write SLE254 Genetics and Genomics assessment answers.
The aforementioned Australian universities are renowned for their quality of teaching and research, and they offer bachelor, master and doctoral programs in genetics and genomics. Thus, they supply the foundation and advanced studies in the respective field.
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Most Australian universities’ course structure for undergraduate studies in genetics and genomics has been divided into three levels. The subjects covered in each group are mentioned below:
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On successful completion of the course, students can:
The completion of the related course in genetics and genomics could lead to the following career opportunities:
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Several discussion forums like Anthrogenica, Reddit-Genetics, genes and genome, Youth4work-Genetics, Science Forums-Genetics, etc., are well-moderated and premier online destinations to get in touch with researchers, geneticists, or scientists worldwide. The community is highly knowledgeable and active and usually discuss topics like DNA replication, mechanism of gene expression, Mendelian genetics, and other related topics. They also provide access to numerous events and services for the understanding, development, and practice, especially for subscribers worldwide.
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Genome-wide association studies are a new method for scientists to determine the genes responsible for human disease. This particular method identifies the genome for a minute or small variations, known as SNPs (single nucleotide polymorphisms) which tend to appear with more frequency in people possessing a specific disease compared to people without having any disease (Tam et al., 2019). Each of these studies identifies hundreds and thousands of SNPs at one time. Researchers or scientists employ data from such studies to pinpoint those genes contributing to an individual’s risk of developing a particular disease (Lee et al., 2018).
The studies of genome-wide association scrutinise SNPs across the genome. Thus, they represent the most appropriate means to identify the complex and usual diseases wherein numerous genetic variations lead to an individual’s risk. The approach has already been investigated in several studies and found SNPs correlate with various complex conditions such as heart abnormalities, diabetes, Crohn disease, and Parkinson's Disease (Mills et al., 2019). According to our highly-proficient academic tutors, future research on genome-wide association will discover more SNPs linked with chronic diseases and variations that pose an impact on an individual’s response to specific drugs and interactions between an individual’s genes and environment.
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Lee, J. J., Wedow, R., Okbay, A., Kong, E., Maghzian, O., Zacher, M., ... & Cesarini, D. (2018). Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals.Nature genetics,50(8), 1112-1121.
Mills, M. C., & Rahal, C. (2019). A scientometric review of genome-wide association studies.Communications Biology,2(1), 1-11.
Tam, V., Patel, N., Turcotte, M., Bossé, Y., Paré, G., & Meyre, D. (2019). Benefits and limitations of genome-wide association studies.Nature Reviews Genetics,20(8), 467-484.
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