Jamie J. Alnasir

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Imperial College London
Country flagUnited Kingdom

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Recent Grants

Grant: Close

[British Council, Travel Award]: Presenting at Workshop - Big Data Analytics Training, MSTI ENSIAS

Open Date: 2015-05-01

Close Date: 2015-05-01

Grant: Close

[British Council, Travel Award]: Presenting at Workshop - Developing data driven Biology in Morocco

Open Date: 2015-02-01

Close Date: 2015-02-01

Grant: Close

[Research Data Alliance, Travel Award]: Presenting at Workshop - RDA Europe 5th Plenary at the San Diego Supercomputing centre.

Open Date: 2015-02-01

Close Date: 2015-02-01

Grant: Close

[Crossland Ph.D. Scholarship]: Analysis of Biological Datasets Utilising Distributed Computing

Open Date: 2013-01-01

Close Date: 2017-01-01

Articles (6)

The yearly global production of data is growing exponentially, outpacing the capacity of existing storage media, such as tape and disk, and surpassing our ability to store it. DNA storage—the representation of arbitrary information as sequences of nucleotides—offers a promising storage medium. DNA is nature’s information-storage molecule of choice and has a number of key properties: It is extremely dense, offering the theoretical possibility of storing 455 EB/g; it is durable, with a half-life of approximately 520 years that can be increased to thousands of years when DNA is chilled and stored dry; and it is amenable to automated synthesis and sequencing. Furthermore, biochemical processes that act on DNA potentially enable highly parallel data manipulation. While biological information is encoded in DNA via a specific mapping from triplet sequences of nucleotides to amino acids, DNA storage is not limited to a single encoding scheme, and there are many possible ways to map data to chemical sequences of nucleotides for synthesis, storage, retrieval, and data manipulation. However, there are several biological, error-tolerance, and information-retrieval considerations that an encoding scheme needs to address to be viable. This comprehensive review focuses on comparing existing work done in encoding arbitrary data within DNA in terms of their encoding schemes, methods to address biological constraints, and measures to provide error correction. We compare encoding approaches on the overall information density and coverage they achieve, as well as the data-retrieval method they use (i.e., sequential or random access). We also discuss the background and evolution of the encoding schemes.

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2023

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2023

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2021

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2021

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2020

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2020

Collaborators (1)

Thomas Heinis

Imperial College London

UNITED KINGDOM
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