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36 Views • Jul 24, 2023 • Click to toggle off description
To treat cancers, we have to better understand them – and their DNA. Previously, DNA would be chopped into thousands of shorter sections. Each shorter section, or read, would be sequenced, and variants within those sections analysed. This is called short-read sequencing.

We are now exploring the clinical potential of a new technique to sequence very long strands of individual DNA without the need to slice it up. This is long-read sequencing.

Emma McCargow, our Programme Lead for Cancer, explains long-read sequencing and how it might help in cancer diagnosis and treatment. 

Long-read sequencing can reveal new information about whole regions and large structural features of the genome that were previously inaccessible to traditional sequencing.

Want more info on this technology and how it's changing our understanding of cancer? Listen to our podcast with Emma, where she dives a bit deeper into long-read v. short-read sequencing: genomicsengland.podbean.com/e/emma-mccargow-genomi…

For more about genomics, visit our understanding genomics webpage: bit.ly/understanding-genomics
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Genre: Science & Technology
Uploaded At Jul 24, 2023 ^^


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RYD date created : 2023-07-24T14:15:00.776909Z
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Top Comments of this video!! :3

@adityasharma9561

5 months ago

Thank you for your valuable input, it made me clear

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@Halabeast

5 months ago

How is pacbio vs its competitors?

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