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Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters
BACKGROUND: Computing alignments between two or more sequences are common operations frequently performed in computational molecular biology. The continuing growth of biological sequence databases establishes the need for their efficient parallel implementation on modern accelerators. RESULTS: This...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959381/ https://www.ncbi.nlm.nih.gov/pubmed/27455061 http://dx.doi.org/10.1186/s12859-016-1128-0 |
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author | Lan, Haidong Chan, Yuandong Xu, Kai Schmidt, Bertil Peng, Shaoliang Liu, Weiguo |
author_facet | Lan, Haidong Chan, Yuandong Xu, Kai Schmidt, Bertil Peng, Shaoliang Liu, Weiguo |
author_sort | Lan, Haidong |
collection | PubMed |
description | BACKGROUND: Computing alignments between two or more sequences are common operations frequently performed in computational molecular biology. The continuing growth of biological sequence databases establishes the need for their efficient parallel implementation on modern accelerators. RESULTS: This paper presents new approaches to high performance biological sequence database scanning with the Smith-Waterman algorithm and the first stage of progressive multiple sequence alignment based on the ClustalW heuristic on a Xeon Phi-based compute cluster. Our approach uses a three-level parallelization scheme to take full advantage of the compute power available on this type of architecture; i.e. cluster-level data parallelism, thread-level coarse-grained parallelism, and vector-level fine-grained parallelism. Furthermore, we re-organize the sequence datasets and use Xeon Phi shuffle operations to improve I/O efficiency. CONCLUSIONS: Evaluations show that our method achieves a peak overall performance up to 220 GCUPS for scanning real protein sequence databanks on a single node consisting of two Intel E5-2620 CPUs and two Intel Xeon Phi 7110P cards. It also exhibits good scalability in terms of sequence length and size, and number of compute nodes for both database scanning and multiple sequence alignment. Furthermore, the achieved performance is highly competitive in comparison to optimized Xeon Phi and GPU implementations. Our implementation is available at https://github.com/turbo0628/LSDBS-mpi. |
format | Online Article Text |
id | pubmed-4959381 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-49593812016-08-01 Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters Lan, Haidong Chan, Yuandong Xu, Kai Schmidt, Bertil Peng, Shaoliang Liu, Weiguo BMC Bioinformatics Research BACKGROUND: Computing alignments between two or more sequences are common operations frequently performed in computational molecular biology. The continuing growth of biological sequence databases establishes the need for their efficient parallel implementation on modern accelerators. RESULTS: This paper presents new approaches to high performance biological sequence database scanning with the Smith-Waterman algorithm and the first stage of progressive multiple sequence alignment based on the ClustalW heuristic on a Xeon Phi-based compute cluster. Our approach uses a three-level parallelization scheme to take full advantage of the compute power available on this type of architecture; i.e. cluster-level data parallelism, thread-level coarse-grained parallelism, and vector-level fine-grained parallelism. Furthermore, we re-organize the sequence datasets and use Xeon Phi shuffle operations to improve I/O efficiency. CONCLUSIONS: Evaluations show that our method achieves a peak overall performance up to 220 GCUPS for scanning real protein sequence databanks on a single node consisting of two Intel E5-2620 CPUs and two Intel Xeon Phi 7110P cards. It also exhibits good scalability in terms of sequence length and size, and number of compute nodes for both database scanning and multiple sequence alignment. Furthermore, the achieved performance is highly competitive in comparison to optimized Xeon Phi and GPU implementations. Our implementation is available at https://github.com/turbo0628/LSDBS-mpi. BioMed Central 2016-07-19 /pmc/articles/PMC4959381/ /pubmed/27455061 http://dx.doi.org/10.1186/s12859-016-1128-0 Text en © The Author(s) 2016 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 Lan, Haidong Chan, Yuandong Xu, Kai Schmidt, Bertil Peng, Shaoliang Liu, Weiguo Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title | Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title_full | Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title_fullStr | Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title_full_unstemmed | Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title_short | Parallel algorithms for large-scale biological sequence alignment on Xeon-Phi based clusters |
title_sort | parallel algorithms for large-scale biological sequence alignment on xeon-phi based clusters |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4959381/ https://www.ncbi.nlm.nih.gov/pubmed/27455061 http://dx.doi.org/10.1186/s12859-016-1128-0 |
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