带相似性矩阵的邻接约束层次聚类及其在基因组学中的应用。

IF 1.5 4区 生物学 Q4 BIOCHEMICAL RESEARCH METHODS
Algorithms for Molecular Biology Pub Date : 2019-11-15 eCollection Date: 2019-01-01 DOI:10.1186/s13015-019-0157-4
Christophe Ambroise, Alia Dehman, Pierre Neuvial, Guillem Rigaill, Nathalie Vialaneix
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引用次数: 21

摘要

背景:基因组数据分析,如全基因组关联研究(GWAS)或Hi-C研究,经常面临基于高分辨率基因座水平测量的相似矩阵将染色体划分为连续区域的问题。一种直观的方法是执行修改的层次聚集聚类(HAC),其中只允许合并相邻的聚类(根据染色体内位置的排序)。但这种方法的一个主要实际缺点是其基因座数量的二次型时间和空间复杂性,每个染色体的基因座数量通常在104到105的数量级。结果:通过假设物理距离遥远的对象之间的相似性可以忽略不计,我们能够提出一种具有拟线性复杂度的邻接约束HAC的实现。这是通过预先计算特定的相似性总和,并将候选融合存储在最小堆中来实现的。我们在GWAS和Hi-C数据集上的插图证明了这一假设的相关性,并表明这种方法突出了具有生物学意义的信号。由于其占用的时间和内存较小,该方法可以在标准笔记本电脑上运行几分钟甚至几秒钟。可用性和实施:软件和样本数据以R包adjcluster的形式提供,可从综合R档案网络(CRAN)下载。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Adjacency-constrained hierarchical clustering of a band similarity matrix with application to genomics.

Adjacency-constrained hierarchical clustering of a band similarity matrix with application to genomics.

Adjacency-constrained hierarchical clustering of a band similarity matrix with application to genomics.

Adjacency-constrained hierarchical clustering of a band similarity matrix with application to genomics.

Background: Genomic data analyses such as Genome-Wide Association Studies (GWAS) or Hi-C studies are often faced with the problem of partitioning chromosomes into successive regions based on a similarity matrix of high-resolution, locus-level measurements. An intuitive way of doing this is to perform a modified Hierarchical Agglomerative Clustering (HAC), where only adjacent clusters (according to the ordering of positions within a chromosome) are allowed to be merged. But a major practical drawback of this method is its quadratic time and space complexity in the number of loci, which is typically of the order of 10 4 to 10 5 for each chromosome.

Results: By assuming that the similarity between physically distant objects is negligible, we are able to propose an implementation of adjacency-constrained HAC with quasi-linear complexity. This is achieved by pre-calculating specific sums of similarities, and storing candidate fusions in a min-heap. Our illustrations on GWAS and Hi-C datasets demonstrate the relevance of this assumption, and show that this method highlights biologically meaningful signals. Thanks to its small time and memory footprint, the method can be run on a standard laptop in minutes or even seconds.

Availability and implementation: Software and sample data are available as an R package, adjclust, that can be downloaded from the Comprehensive R Archive Network (CRAN).

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来源期刊
Algorithms for Molecular Biology
Algorithms for Molecular Biology 生物-生化研究方法
CiteScore
2.40
自引率
10.00%
发文量
16
审稿时长
>12 weeks
期刊介绍: Algorithms for Molecular Biology publishes articles on novel algorithms for biological sequence and structure analysis, phylogeny reconstruction, and combinatorial algorithms and machine learning. Areas of interest include but are not limited to: algorithms for RNA and protein structure analysis, gene prediction and genome analysis, comparative sequence analysis and alignment, phylogeny, gene expression, machine learning, and combinatorial algorithms. Where appropriate, manuscripts should describe applications to real-world data. However, pure algorithm papers are also welcome if future applications to biological data are to be expected, or if they address complexity or approximation issues of novel computational problems in molecular biology. Articles about novel software tools will be considered for publication if they contain some algorithmically interesting aspects.
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