Genome Sequences analysis using HMM in Biological Databases

Manas Ranjan Pradhan
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引用次数: 1

Abstract

There are variety of problems exist in molecular biology. The sequenced genomes generally give information about to understand the underlying mechanisms of various biological functions in cells. However, as data is available enormously, it is really difficult to analyze them without the help of computational methods. In order to extract meaningful information from the data, we need computational techniques to biological sequence analysis. Due to digitization, the biological databases are continuously improved and updated. In other hand many Biological Databases are available which are classified as primary, secondary and composite type. While we do sequence analysis, we analyze in terms of functional or structural analysis. The hidden data certain time could not reflect in databases which may have vital role in analyzing biological results. The HMM (Hidden Markov Model) is one of the application area of artificial intelligence technique to model data analysis features. This research work here focuses on modeling DNA sequencing error with HMM by identifying hidden data from various depository of molecular databases which will help in re-sequencing genome data.
基于HMM的生物数据库基因组序列分析
分子生物学中存在着各种各样的问题。测序的基因组通常提供有关了解细胞中各种生物功能的潜在机制的信息。然而,由于数据非常多,如果没有计算方法的帮助,很难对它们进行分析。为了从数据中提取有意义的信息,我们需要计算技术来进行生物序列分析。由于数字化,生物数据库不断得到改进和更新。另一方面,许多生物数据库可分为初级、二级和复合型。当我们做序列分析时,我们根据功能或结构分析进行分析。隐藏的数据在一定时间内无法在数据库中反映出来,而这些数据对分析生物学结果可能具有至关重要的作用。隐马尔可夫模型是人工智能技术对数据分析特征进行建模的应用领域之一。本研究的重点是利用隐马尔可夫模型来识别各种分子数据库中的隐藏数据,从而对DNA测序误差进行建模,这将有助于基因组数据的重测序。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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