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首页> 外文期刊>Journal of Bioinformatics and Computational Biology >FPQRNA: HARDWARE-ACCELERATED QRNA PACKAGE FOR NONCODING RNA GENE DETECTING ON FPGA
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FPQRNA: HARDWARE-ACCELERATED QRNA PACKAGE FOR NONCODING RNA GENE DETECTING ON FPGA

机译:FPQRNA:硬件加速的QRNA包装,用于在FPGA上进行非编码RNA基因检测

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摘要

Noncoding RNAs (ncRNAs) have important functional roles in biological processes and have become a central research interest in modern molecular biology. However, how to find ncRNA attracts much more attention since ncRNA gene sequences do not have strong statistical signals, unlike protein coding genes. QRNA is a powerful program and has been widely used as an efficient analysis tool to detect ncRNA gene at present. Unfortunately, the O(L3) computing requirements and complicated data dependency greatly limit the usefulness of QRNA package with the explosion in gene database. In this paper, we present a fine-grained parallel QRNA prototype system, FPQRNA, for accelerating ncRNA gene detection application on FPGA chip. We propose a systolic-like array architecture with multiple PEs (Processing Elements). We partition the tasks by columns and assign tasks to PEs for load balance. We exploit data reuse schemes to reduce the need to load matrices from external memory. The experimental results show a speedup factor of more than 18× over the QRNA - 2.0.3c software running on a PC platform with AMD Phenom 9650 Quad CPU for pairwise sequence alignment with 996 residues, however the power consumption of our FPGA accelerator is only about 30% of that of the general-purpose microprocessors.
机译:非编码RNA(ncRNA)在生物学过程中具有重要的功能,并已成为现代分子生物学的主要研究热点。但是,由于ncRNA基因序列不像蛋白质编码基因那样具有强大的统计信号,因此如何找到ncRNA引起了更多的关注。 QRNA是功能强大的程序,目前已广泛用作检测ncRNA基因的有效分析工具。不幸的是,随着基因数据库的爆炸式增长,O(L3)的计算要求和复杂的数据依赖性极大地限制了QRNA包装的实用性。在本文中,我们提出了一种细粒度的并行QRNA原型系统FPQRNA,用于加快FPGA芯片上ncRNA基因检测的应用。我们提出了具有多个PE(处理元素)的类似收缩压的阵列架构。我们按列划分任务,并将任务分配给PE以实现负载平衡。我们利用数据重用方案来减少从外部存储器加载矩阵的需求。实验结果表明,在运行有AMD Phenom 9650 Quad CPU的PC平台上运行的QRNA-2.0.3c软件的加速因子提高了18倍,实现了996个残基的成对序列比对,但是我们的FPGA加速器的功耗仅为通用微处理器的30%。

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