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GVC: efficient random access compression for gene sequence variations
BACKGROUND: In recent years, advances in high-throughput sequencing technologies have enabled the use of genomic information in many fields, such as precision medicine, oncology, and food quality control. The amount of genomic data being generated is growing rapidly and is expected to soon surpass t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044409/ https://www.ncbi.nlm.nih.gov/pubmed/36978010 http://dx.doi.org/10.1186/s12859-023-05240-0 |
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author | Adhisantoso, Yeremia Gunawan Voges, Jan Rohlfing, Christian Tunev, Viktor Ohm, Jens-Rainer Ostermann, Jörn |
author_facet | Adhisantoso, Yeremia Gunawan Voges, Jan Rohlfing, Christian Tunev, Viktor Ohm, Jens-Rainer Ostermann, Jörn |
author_sort | Adhisantoso, Yeremia Gunawan |
collection | PubMed |
description | BACKGROUND: In recent years, advances in high-throughput sequencing technologies have enabled the use of genomic information in many fields, such as precision medicine, oncology, and food quality control. The amount of genomic data being generated is growing rapidly and is expected to soon surpass the amount of video data. The majority of sequencing experiments, such as genome-wide association studies, have the goal of identifying variations in the gene sequence to better understand phenotypic variations. We present a novel approach for compressing gene sequence variations with random access capability: the Genomic Variant Codec (GVC). We use techniques such as binarization, joint row- and column-wise sorting of blocks of variations, as well as the image compression standard JBIG for efficient entropy coding. RESULTS: Our results show that GVC provides the best trade-off between compression and random access compared to the state of the art: it reduces the genotype information size from 758 GiB down to 890 MiB on the publicly available 1000 Genomes Project (phase 3) data, which is 21% less than the state of the art in random-access capable methods. CONCLUSIONS: By providing the best results in terms of combined random access and compression, GVC facilitates the efficient storage of large collections of gene sequence variations. In particular, the random access capability of GVC enables seamless remote data access and application integration. The software is open source and available at https://github.com/sXperfect/gvc/. |
format | Online Article Text |
id | pubmed-10044409 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100444092023-03-29 GVC: efficient random access compression for gene sequence variations Adhisantoso, Yeremia Gunawan Voges, Jan Rohlfing, Christian Tunev, Viktor Ohm, Jens-Rainer Ostermann, Jörn BMC Bioinformatics Research BACKGROUND: In recent years, advances in high-throughput sequencing technologies have enabled the use of genomic information in many fields, such as precision medicine, oncology, and food quality control. The amount of genomic data being generated is growing rapidly and is expected to soon surpass the amount of video data. The majority of sequencing experiments, such as genome-wide association studies, have the goal of identifying variations in the gene sequence to better understand phenotypic variations. We present a novel approach for compressing gene sequence variations with random access capability: the Genomic Variant Codec (GVC). We use techniques such as binarization, joint row- and column-wise sorting of blocks of variations, as well as the image compression standard JBIG for efficient entropy coding. RESULTS: Our results show that GVC provides the best trade-off between compression and random access compared to the state of the art: it reduces the genotype information size from 758 GiB down to 890 MiB on the publicly available 1000 Genomes Project (phase 3) data, which is 21% less than the state of the art in random-access capable methods. CONCLUSIONS: By providing the best results in terms of combined random access and compression, GVC facilitates the efficient storage of large collections of gene sequence variations. In particular, the random access capability of GVC enables seamless remote data access and application integration. The software is open source and available at https://github.com/sXperfect/gvc/. BioMed Central 2023-03-28 /pmc/articles/PMC10044409/ /pubmed/36978010 http://dx.doi.org/10.1186/s12859-023-05240-0 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Adhisantoso, Yeremia Gunawan Voges, Jan Rohlfing, Christian Tunev, Viktor Ohm, Jens-Rainer Ostermann, Jörn GVC: efficient random access compression for gene sequence variations |
title | GVC: efficient random access compression for gene sequence variations |
title_full | GVC: efficient random access compression for gene sequence variations |
title_fullStr | GVC: efficient random access compression for gene sequence variations |
title_full_unstemmed | GVC: efficient random access compression for gene sequence variations |
title_short | GVC: efficient random access compression for gene sequence variations |
title_sort | gvc: efficient random access compression for gene sequence variations |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10044409/ https://www.ncbi.nlm.nih.gov/pubmed/36978010 http://dx.doi.org/10.1186/s12859-023-05240-0 |
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