MemAlign:加速基因测序的记忆结构

Meysam Roodi, A. Moshovos
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引用次数: 0

摘要

自2003年人类参考基因组被发现以来,一些应用发现基因测序是一种很有前途的机制,可以帮助改善它们的结果。其中包括研究遗传疾病、产前监测等。基因测序的典型配置包括几个复杂的处理阶段,每个阶段都由一个单独的软件包执行。中间结果在基因测序的不同步骤之间通过大文件传输,因此基因测序是一项处理和I/O要求很高的任务。利用先进的内存速度和容量,以流水线化基因测序步骤和避免使用文件存储来通信中间结果的最终目标,本文提出了MemAlign,一种新的预排序内存结构,以流水线化基因测序的第一和第二处理步骤;对齐和排序。MemAlign的记忆位置数量与人类参考基因组的位置相对应。与压缩对齐结果的技术相结合,MemAlign通过将对齐结果存储在与对齐位置对应的内存位置中,实质上消除了Sort步骤。MemAlign不仅加快了Alignment和Sort的组合处理时间,而且还节省了存储这两个步骤之间的中间结果所需的大量存储空间。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MemAlign: A Memory Structure to Accelerate Gene Sequencing
Since 2003, when the human reference genome was discovered, several applications found gene sequencing a promising mechanism to help improve their results. These include studying hereditary diseases, prenatal monitoring and others. Gene sequencing in its typical configuration consists of several elaborate processing stages, each performed by a separate software package. The intermediate results are transferred via large files between gene sequencing different steps, hence making gene sequencing a processing and I/O demanding task. Taking advantage of advances memory speed and capacity and with the ultimate goal of pipelining the gene sequencing steps and avoiding utilizing file storage to communicate intermediate results, in this paper we present MemAlign, a novel pre-sorted memory structure to pipeline the first and second processing steps of gene sequencing; Alignment and Sort. The number of memory locations of MemAlign corresponds the positions on the human reference genome. Combined with techniques to compress the alignment results, MemAlign essentially eliminates the Sort step by storing alignment results in the memory location that corresponds to the alignment position. MemAlign not only speeds up the combined processing time of Alignment and Sort, but also saves the considerable amount of storage required to store the intermediate results between the two steps.
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