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Predictive Genome Analysis Using Partial DNA Sequencing Data

机译:使用部分DNA测序数据预测基因组分析

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Much research has been dedicated to reducing the computational time associated with the analysis of genome data, which resulted in shifting the bottleneck from the time needed for the computational analysis part to the actual time needed for sequencing of DNA information. DNA sequencing is a time consuming process, and all existing DNA analysis methods have to wait for the DNA sequencing to completely finish before starting the analysis. In this paper, we propose a new DNA analysis approach where we start the genome analysis before the DNA sequencing is completely finished. The genome analysis is started when the DNA reads are still in the process of being sequenced. We use algorithms to predict the unknown bases and their corresponding base quality scores of the incomplete read. Results show that our method of predicting the unknown bases and quality scores achieves more than 90% similarity with the full dataset for 50 unknown bases (slashing more than a day of sequencing time). We also show that our base quality value prediction scheme is highly accurate, only reducing the similarity of the detected variants by 0.45%. However, there is still room to introduce more accurate prediction schemes for the unknown bases to increase the effectiveness of the analysis by up to 5.8%.
机译:许多研究一直致力于减少与基因组数据分析相关的计算时间,这导致从计算分析部分的瓶颈移位到DNA信息测序所需的实际时间。 DNA测序是耗时的过程,并且所有现有的DNA分析方法必须在开始分析之前等待DNA测序完全完成。在本文中,我们提出了一种新的DNA分析方法,在DNA测序完全完成之前开始基因组分析。当DNA读数仍处于测序的过程时,开始基因组分析。我们使用算法预测未完成读取的未知基础及其相应的基本质量分数。结果表明,我们预测未知基地和质量评分的方法与50个未知基座的完整数据集相似于90多个相似性(削减了超过一天的排序时间)。我们还表明,我们的基础质量值预测方案高度准确,只能将检测到的变体的相似性降低0.45 %。然而,仍有空间为未知基础引入更准确的预测方案,以将分析的有效性增加到5.8%。

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