Abstract

BackgroundPairwise statistical significance has been recognized to be able to accurately identify related sequences, which is a very important cornerstone procedure in numerous bioinformatics applications. However, it is both computationally and data intensive, which poses a big challenge in terms of performance and scalability.ResultsWe present a GPU implementation to accelerate pairwise statistical significance estimation of local sequence alignment using standard substitution matrices. By carefully studying the algorithm's data access characteristics, we developed a tile-based scheme that can produce a contiguous data access in the GPU global memory and sustain a large number of threads to achieve a high GPU occupancy. We further extend the parallelization technique to estimate pairwise statistical significance using position-specific substitution matrices, which has earlier demonstrated significantly better sequence comparison accuracy than using standard substitution matrices. The implementation is also extended to take advantage of dual-GPUs. We observe end-to-end speedups of nearly 250 (370) × using single-GPU Tesla C2050 GPU (dual-Tesla C2050) over the CPU implementation using Intel© Core™i7 CPU 920 processor.ConclusionsHarvesting the high performance of modern GPUs is a promising approach to accelerate pairwise statistical significance estimation for local sequence alignment.

Highlights

  • Pairwise statistical significance has been recognized to be able to accurately identify related sequences, which is a very important cornerstone procedure in numerous bioinformatics applications

  • We observe that permutation presents high degrees of data independency that are naturally suitable for single-instruction, multiple-thread (SIMT) architectures [38] and can be mapped very well to task parallelism models of Graphics Processing Unit (GPU)

  • We can obtain some hints about improving the performance by analyzing the single-pair Pairwise Statistical Significance Estimation (PSSE) implementation

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Summary

Introduction

Pairwise statistical significance has been recognized to be able to accurately identify related sequences, which is a very important cornerstone procedure in numerous bioinformatics applications. It is both computationally and data intensive, which poses a big challenge in terms of performance and scalability. One of the most widely used procedures for extracting information from proteomic and genomic data is pairwise sequence alignment (PSA). PSA finds the extent of similarity between them. Accurate estimation of statistical significance of gapped sequence alignment has attracted a lot of research in recent years [13,14,15,16,17,18,19,20,21,22,23,24,25,26]

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