Sievers Aaron, Bosiek Katharina, Bisch Marc, Dreessen Chris, Riedel Jascha, Froß Patrick, Hausmann Michael, Hildenbrand Georg
Kirchhoff-Institute for Physics, Heidelberg University, INF 227, 69117 Heidelberg, Germany.
Department of Radiation Oncology, Universitätsmedizin Mannheim, Medical Faculty Mannheim, Heidelberg University, Theodor-Kutzer-Ufer 1-3, 68167 Mannheim, Germany.
Genes (Basel). 2017 Apr 19;8(4):122. doi: 10.3390/genes8040122.
In genome analysis, -based comparison methods have become standard tools. However, even though they are able to deliver reliable results, other algorithms seem to work better in some cases. To improve -mer-based DNA sequence analysis and comparison, we successfully checked whether adding positional resolution is beneficial for finding and/or comparing interesting organizational structures. A simple but efficient algorithm for extracting and saving local -mer spectra (frequency distribution of -mers) was developed and used. The results were analyzed by including positional information based on visualizations as genomic maps and by applying basic vector correlation methods. This analysis was concentrated on small word lengths (1 ≤ ≤ 4) on relatively small viral genomes of and , while also checking its usability for larger sequences, namely human chromosome 2 and the homologous chromosomes (2A, 2B) of a chimpanzee. Using this alignment-free analysis, several regions with specific characteristics in and formerly identified by independent, mostly alignment-based methods, were confirmed. Correlations between the -mer content and several genes in these genomes have been found, showing similarities between classified and unclassified viruses, which may be potentially useful for further taxonomic research. Furthermore, unknown -mer correlations in the genomes of Human Herpesviruses (HHVs), which are probably of major biological function, are found and described. Using the chromosomes of a chimpanzee and human that are currently known, identities between the species on every analyzed chromosome were reproduced. This demonstrates the feasibility of our approach for large data sets of complex genomes. Based on these results, we suggest -mer analysis with positional resolution as a method for closing a gap between the effectiveness of alignment-based methods (like NCBI BLAST) and the high pace of standard -mer analysis.
在基因组分析中,基于 - 聚体的比较方法已成为标准工具。然而,尽管它们能够提供可靠的结果,但其他算法在某些情况下似乎效果更好。为了改进基于 - 聚体的DNA序列分析和比较,我们成功检验了添加位置分辨率对于发现和/或比较有趣的组织结构是否有益。我们开发并使用了一种简单而高效的算法来提取和保存局部 - 聚体谱(- 聚体的频率分布)。通过将基于可视化的位置信息纳入基因组图谱,并应用基本的向量相关方法来分析结果。该分析集中在长度为1≤ ≤4的小单词长度上,针对相对较小的 和 的病毒基因组,同时也检验了其对较大序列(即人类2号染色体和黑猩猩的同源染色体(2A、2B))的适用性。使用这种无需比对的分析方法,通过独立的、大多基于比对的方法先前鉴定出的 和 中具有特定特征的几个区域得到了确认。已经发现了这些基因组中 - 聚体含量与几个基因之间的相关性,显示了分类病毒和未分类病毒之间的相似性,这可能对进一步的分类学研究有潜在帮助。此外,还发现并描述了人类疱疹病毒(HHV)基因组中可能具有主要生物学功能的未知 - 聚体相关性。利用目前已知的黑猩猩和人类的染色体,再现了每个分析染色体上物种之间的一致性。这证明了我们的方法对于复杂基因组大数据集的可行性。基于这些结果,我们建议将具有位置分辨率的 - 聚体分析作为一种方法,以弥合基于比对的方法(如NCBI BLAST)的有效性与标准 - 聚体分析的高速度之间的差距。