%0 Journal Article
%T Modern Computational Techniques for the HMMER Sequence Analysis
%A Xiandong Meng
%A Yanqing Ji
%J ISRN Bioinformatics
%D 2013
%R 10.1155/2013/252183
%X This paper focuses on the latest research and critical reviews on modern computing architectures, software and hardware accelerated algorithms for bioinformatics data analysis with an emphasis on one of the most important sequence analysis applications¡ªhidden Markov models (HMM). We show the detailed performance comparison of sequence analysis tools on various computing platforms recently developed in the bioinformatics society. The characteristics of the sequence analysis, such as data and compute-intensive natures, make it very attractive to optimize and parallelize by using both traditional software approach and innovated hardware acceleration technologies. 1. Introduction At the beginning of the 21st century, an explosion of information was discovered from the living organisms, especially in areas of molecular biology and genetics. The focus of bioinformatics deals with this flood of information, which comes from academy, industry, and government labs, and turning it into useful knowledge. Bioinformatics is important to a virtually unlimited number of fields. As the genetic information being organized into computerized databases and their sizes steadily grow, molecular biologists need effective and efficient computational tools to store and retrieve the cognate information such as biological information from the databases, to analyze the sequence patterns they contain, and to extract the biological knowledge the sequences contain. The field of bioinformatics computing is advancing at an unprecedented rate. For people working with genomics and high-throughput sequencing data analysis, it is a serious challenge to analyze the vast amounts of data coming from the next generation sequencing (NGS) instruments. For example, there were approximately 126,£¿551,£¿501, and 141 bases in 135,£¿440, and 924 sequence records in the traditional GenBank divisions as of April 2011 [1]. The tendency is likely only to be reinforced by new generation sequencers, for example, Illumina HiSeq 2500 generating up to 120£¿Gb of data in 17 hours per run [2]. Data in itself is almost useless until it is analyzed and correctly interpreted. The draft of the human genome has given us a genetic list of what is necessary for building a human: approximately 35,000 genes. For a genome as large as the human genome, it may take many days of CPU time on large-memory, multiprocessor computers to analyze. To handle this much data, computational strategies are important to tackle this vital bottleneck, which can aid scientists in the extraction of useful and important biological data.
%U http://www.hindawi.com/journals/isrn.bioinformatics/2013/252183/