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SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences
BACKGROUND: The Smith-Waterman (SW) algorithm is the best choice for searching similar regions between two DNA or protein sequences. However, it may become impracticable in some contexts due to its high computational demands. Consequently, the computer science community has focused on the use of mod...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245597/ https://www.ncbi.nlm.nih.gov/pubmed/30458766 http://dx.doi.org/10.1186/s12918-018-0614-6 |
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author | Rucci, Enzo Garcia, Carlos Botella, Guillermo De Giusti, Armando Naiouf, Marcelo Prieto-Matias, Manuel |
author_facet | Rucci, Enzo Garcia, Carlos Botella, Guillermo De Giusti, Armando Naiouf, Marcelo Prieto-Matias, Manuel |
author_sort | Rucci, Enzo |
collection | PubMed |
description | BACKGROUND: The Smith-Waterman (SW) algorithm is the best choice for searching similar regions between two DNA or protein sequences. However, it may become impracticable in some contexts due to its high computational demands. Consequently, the computer science community has focused on the use of modern parallel architectures such as Graphics Processing Units (GPUs), Xeon Phi accelerators and Field Programmable Gate Arrays (FGPAs) to speed up large-scale workloads. RESULTS: This paper presents and evaluates SWIFOLD: a Smith-Waterman parallel Implementation on FPGA with OpenCL for Long DNA sequences. First, we evaluate its performance and resource usage for different kernel configurations. Next, we carry out a performance comparison between our tool and other state-of-the-art implementations considering three different datasets. SWIFOLD offers the best average performance for small and medium test sets, achieving a performance that is independent of input size and sequence similarity. In addition, SWIFOLD provides competitive performance rates in comparison with GPU-based implementations on the latest GPU generation for the large dataset. CONCLUSIONS: The results suggest that SWIFOLD can be a serious contender for accelerating the SW alignment of DNA sequences of unrestricted size in an affordable way reaching on average 125 GCUPS and almost a peak of 270 GCUPS. |
format | Online Article Text |
id | pubmed-6245597 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62455972018-11-26 SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences Rucci, Enzo Garcia, Carlos Botella, Guillermo De Giusti, Armando Naiouf, Marcelo Prieto-Matias, Manuel BMC Syst Biol Research BACKGROUND: The Smith-Waterman (SW) algorithm is the best choice for searching similar regions between two DNA or protein sequences. However, it may become impracticable in some contexts due to its high computational demands. Consequently, the computer science community has focused on the use of modern parallel architectures such as Graphics Processing Units (GPUs), Xeon Phi accelerators and Field Programmable Gate Arrays (FGPAs) to speed up large-scale workloads. RESULTS: This paper presents and evaluates SWIFOLD: a Smith-Waterman parallel Implementation on FPGA with OpenCL for Long DNA sequences. First, we evaluate its performance and resource usage for different kernel configurations. Next, we carry out a performance comparison between our tool and other state-of-the-art implementations considering three different datasets. SWIFOLD offers the best average performance for small and medium test sets, achieving a performance that is independent of input size and sequence similarity. In addition, SWIFOLD provides competitive performance rates in comparison with GPU-based implementations on the latest GPU generation for the large dataset. CONCLUSIONS: The results suggest that SWIFOLD can be a serious contender for accelerating the SW alignment of DNA sequences of unrestricted size in an affordable way reaching on average 125 GCUPS and almost a peak of 270 GCUPS. BioMed Central 2018-11-20 /pmc/articles/PMC6245597/ /pubmed/30458766 http://dx.doi.org/10.1186/s12918-018-0614-6 Text en © The Author(s) 2018 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver(http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Rucci, Enzo Garcia, Carlos Botella, Guillermo De Giusti, Armando Naiouf, Marcelo Prieto-Matias, Manuel SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title | SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title_full | SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title_fullStr | SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title_full_unstemmed | SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title_short | SWIFOLD: Smith-Waterman implementation on FPGA with OpenCL for long DNA sequences |
title_sort | swifold: smith-waterman implementation on fpga with opencl for long dna sequences |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6245597/ https://www.ncbi.nlm.nih.gov/pubmed/30458766 http://dx.doi.org/10.1186/s12918-018-0614-6 |
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