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BMC Bioinformatics ; 13 Suppl 5: S3, 2012 Apr 12.
Artículo en Inglés | MEDLINE | ID: mdl-22537007

RESUMEN

BACKGROUND: 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. However, it is both computationally and data intensive, which poses a big challenge in terms of performance and scalability. RESULTS: We 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 Corei7 CPU 920 processor. CONCLUSIONS: Harvesting the high performance of modern GPUs is a promising approach to accelerate pairwise statistical significance estimation for local sequence alignment.


Asunto(s)
Gráficos por Computador/instrumentación , Alineación de Secuencia/métodos , Análisis de Secuencia de Proteína/métodos , Algoritmos , Alineación de Secuencia/instrumentación , Análisis de Secuencia de Proteína/instrumentación , Programas Informáticos
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