Genomic Medicine: Harnessing the Power of the Human Genome
Join experts at the University of Glasgow to explore how cutting-edge genomics technologies and analysis tools are changing how we understand and treat medical conditions.
Duration
4 weeks
Weekly study
4 hours
100% online
How it works
Included in an ExpertTrack
Course 2 of 3
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Established
1451
Location
Glasgow, Scotland, UK
World ranking
Source: QS World University Rankings 2020
This course will advance your understanding of the rapidly growing use of genomics in the research, diagnosis, and treatment of clinical conditions.
As medical technology advances, new hugely powerful genomics technologies enable an individual’s full gene set – and even whole genome – to be analysed rapidly and simultaneously, with the aim of identifying pathogenic DNA variants.
On this course, you’ll develop your understanding of the structure, organisation, and function of the human genome, and learn how genetic variants can disturb this function and cause disease.
Alongside leading academics from the University of Glasgow, you’ll explore how genomic analysis enables scientists to extract medically important findings.
You’ll get to grips with genomic data analysis and build your skills in using sophisticated online databases and tools to analyse the latest human genomic datasets.
You’ll also learn common terminology used in global genomic analysis and explore how genomic technologies can be applied in guided therapy for specific medical conditions.
In this activity you'll get the chance to introduce yourself and meet the course team and your fellow learners. You''ll also get an overview of the field of genomics and how it can be used.
In the next couple of steps you will learn about the building blocks of the genome and how we study it.
In this activity we introduce the Ensembl Genome Browser, a powerful tool which will allow you to begin your exploration of the genome.
You can review how you got on this week here and we'll take a look at what is coming next week.
In this activity we explore the different types of variant that are present in the genome and the effect they can have on health and disease.
It's vital that we are able to use a common language to refer to genetic variants. In this activity we discuss how variant naming ensures we're all talking about the same thing!
Now for the practical activity: In the next few steps you will learn how to use online tools to help solve a clinical problem.
You can review how you got on this week here and we'll take a look at what is coming next week.
The first activity this week will cover one of the most important topics in genomics - how the genome can be sequenced.
In the previous activity we learned about how the genome can be sequenced. With this in mind we'll now move on to look at how all this data can be interpreted.
To bring the information you've learned in the last two steps together we now need to look at how to classify the variants we've just investigated. Are they harmful or not?
You can review how you got on this week here and we'll take a look at what is coming next week.
In the first activity this week we will focus on how a knowledge of genomics can be used to guide treatment of a range of conditions.
In the second half of this week we will look at how genomics can guide research into disease - before moving on to look at how it can inform therapy.
We've previously looked at using genomics in researching cancer - in this activity we move on to examine how it can be used in cancer treatment.
In the final activity of the the course, you will have the opportunity to test your knowledge and share your highlights and challenges of the past few weeks.
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