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Predictive Genome Analysis Using Partial DNA Sequencing Data

机译:使用部分DNA测序数据进行预测性基因组分析

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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:大量研究致力于减少与基因组数据分析相关的计算时间,这导致瓶颈从计算分析部分所需的时间转移到DNA信息测序所需的实际时间。 DNA测序是一个耗时的过程,所有现有的DNA分析方法都必须等待DNA测序完全完成后才能开始分析。在本文中,我们提出了一种新的DNA分析方法,即在DNA测序完成之前先进行基因组分析。当DNA读数仍在测序过程中时,便开始进行基因组分析。我们使用算法来预测不完整读物的未知碱基及其对应的碱基质量得分。结果表明,我们预测未知碱基和质量得分的方法与50个未知碱基的完整数据集的相似度达到90%以上(节省了一天的测序时间)。我们还表明,我们的基本质量值预测方案非常准确,仅将检测到的变体的相似性降低了0.45%。但是,仍然存在为未知碱基引入更准确的预测方案的空间,以将分析的有效性提高多达5.8%。

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