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PIO scientist’s work may be key in Covid battle
NGS Can Help Sequence Human Genome For $1k
“We are only scratching the surface of what is possible. It is a long journey… We were surprised to see the benefits it has had on basic research and life sciences… It is exciting to see new creative applications of the technology in journals,” Chennai-born Balasubramanian told TOI.
The origins of NGS go back nearly 25 years when the two were collaborating as independent researchers. “We were not trying to sequence anything or develop technology but the way we were approaching the problem led us to seeing a new way to sequence DNA,” Balasubramanian said. NGS sets up millions of fragments of DNA from a sample on to the surface of a chip in an array. They are then amplified. Each fragment is decoded on that chip using fluorescent coloured nucleotides (building blocks of DNA and RNA). The colour-coded nucleotides are detected over and over, mapping the DNA sequence of each fragment. Because this is done with many fragments at the same time, it is fast, inexpensive and scalable.In 1998, Balasubramanian and Klenerman founded Solexa and put together a team to take what they had found and make the technology workable. In 2006, Illumina acquired Solexa and fine tuned the technology.

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