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A biological sequence comparison algorithm using quantum computers

Genetic information is encoded as linear sequences of nucleotides, represented by letters ranging from thousands to billions. Differences between sequences are identified through comparative approaches like sequence analysis, where variations can occur at the individual nucleotide level or collectiv...

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Autores principales: Kösoglu-Kind, Büsra, Loredo, Robert, Grossi, Michele, Bernecker, Christian, Burks, Jody M., Buchkremer, Rüdiger
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477269/
https://www.ncbi.nlm.nih.gov/pubmed/37666875
http://dx.doi.org/10.1038/s41598-023-41086-5
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author Kösoglu-Kind, Büsra
Loredo, Robert
Grossi, Michele
Bernecker, Christian
Burks, Jody M.
Buchkremer, Rüdiger
author_facet Kösoglu-Kind, Büsra
Loredo, Robert
Grossi, Michele
Bernecker, Christian
Burks, Jody M.
Buchkremer, Rüdiger
author_sort Kösoglu-Kind, Büsra
collection PubMed
description Genetic information is encoded as linear sequences of nucleotides, represented by letters ranging from thousands to billions. Differences between sequences are identified through comparative approaches like sequence analysis, where variations can occur at the individual nucleotide level or collectively due to various phenomena such as recombination or deletion. Detecting these sequence differences is vital for understanding biology and medicine, but the complexity and size of genomic data require substantial classical computing power. Inspired by human visual perception and pixel representation on quantum computers, we leverage these techniques to implement pairwise sequence analysis. Our method utilizes the Flexible Representation of Quantum Images (FRQI) framework, enabling comparisons at a fine granularity to single letters or amino acids within gene sequences. This novel approach enhances accuracy and resolution, surpassing traditional methods by capturing subtle genetic variations with precision. In summary, our approach offers algorithmic advantages, including reduced time complexity, improved space efficiency, and accurate sequence comparisons. The novelty lies in applying the FRQI algorithm to compare quantum images in genome sequencing, allowing for examination at the individual letter or amino acid level. This breakthrough holds promise for advancing biological data analysis and enables a more comprehensive understanding of genetic information.
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spelling pubmed-104772692023-09-06 A biological sequence comparison algorithm using quantum computers Kösoglu-Kind, Büsra Loredo, Robert Grossi, Michele Bernecker, Christian Burks, Jody M. Buchkremer, Rüdiger Sci Rep Article Genetic information is encoded as linear sequences of nucleotides, represented by letters ranging from thousands to billions. Differences between sequences are identified through comparative approaches like sequence analysis, where variations can occur at the individual nucleotide level or collectively due to various phenomena such as recombination or deletion. Detecting these sequence differences is vital for understanding biology and medicine, but the complexity and size of genomic data require substantial classical computing power. Inspired by human visual perception and pixel representation on quantum computers, we leverage these techniques to implement pairwise sequence analysis. Our method utilizes the Flexible Representation of Quantum Images (FRQI) framework, enabling comparisons at a fine granularity to single letters or amino acids within gene sequences. This novel approach enhances accuracy and resolution, surpassing traditional methods by capturing subtle genetic variations with precision. In summary, our approach offers algorithmic advantages, including reduced time complexity, improved space efficiency, and accurate sequence comparisons. The novelty lies in applying the FRQI algorithm to compare quantum images in genome sequencing, allowing for examination at the individual letter or amino acid level. This breakthrough holds promise for advancing biological data analysis and enables a more comprehensive understanding of genetic information. Nature Publishing Group UK 2023-09-04 /pmc/articles/PMC10477269/ /pubmed/37666875 http://dx.doi.org/10.1038/s41598-023-41086-5 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Kösoglu-Kind, Büsra
Loredo, Robert
Grossi, Michele
Bernecker, Christian
Burks, Jody M.
Buchkremer, Rüdiger
A biological sequence comparison algorithm using quantum computers
title A biological sequence comparison algorithm using quantum computers
title_full A biological sequence comparison algorithm using quantum computers
title_fullStr A biological sequence comparison algorithm using quantum computers
title_full_unstemmed A biological sequence comparison algorithm using quantum computers
title_short A biological sequence comparison algorithm using quantum computers
title_sort biological sequence comparison algorithm using quantum computers
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10477269/
https://www.ncbi.nlm.nih.gov/pubmed/37666875
http://dx.doi.org/10.1038/s41598-023-41086-5
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