Shankar Balasubramanian on decoding DNA
The Life Scientific
BBC
4.6 • 1.4K Ratings
🗓️ 8 March 2022
⏱️ 30 minutes
🧾️ Download transcript
Summary
Sir Shankar Balasubramanian is responsible for a revolution in medicine. The method he invented for reading, at speed, the unique genetic code that makes each one of us who we are, is ten million times faster than the technology that was used in the human genome project at the turn of the century. What’s more, it can be done much more cheaply than before and on a desktop machine. And it’s transforming healthcare, by helping us to understand the genetic basis of many diseases (particularly cancers) and to develop new diagnostic tests, medicines and personalised treatments. ‘DNA has never failed to keep me excited and curious’ says Shankar, winner of the highly prestigious 2022 Breakthrough Prize in Life Sciences. He didn’t set out to create a game-changing technology or to make a lot of money. He just wanted to understand the DNA double helix in the greatest possible detail; to reveal how it worked, molecule by molecule. And he still rides a rickety old bicycle to work in Cambridge. Producer: Anna Buckley
Image ©University of Cambridge
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| 1:02.6 | My guest today is responsible for a revolution. |
| 1:06.3 | The ability to read at speed the unique genetic code that makes each one of us who we are |
| 1:12.2 | is transforming healthcare, helping us to understand the genetic basis of many diseases, |
| 1:17.6 | particularly cancers and to develop new diagnostic tests, medicines and personalised treatments. |
| 1:24.7 | Shankar Balasabramanian invented a way of sequencing genomes that is 10 million times faster |
| 1:31.4 | than the technology that was used in the human genome project at the turn of the century. |
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