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探索单倍型解析泛基因组中的基因组内和基因组间变异。

Exploring intra- and intergenomic variation in haplotype-resolved pangenomes.

作者信息

Jonkheer Eef M, de Ridder Dick, van der Lee Theo A J, de Haan Jorn R, Berke Lidija, Smit Sandra

机构信息

Bioinformatics Group, Wageningen University & Research, Wageningen, The Netherlands.

Biointeractions and Plant Health, Wageningen Plant Research, Wageningen, The Netherlands.

出版信息

Plant Biotechnol J. 2025 Mar;23(3):874-886. doi: 10.1111/pbi.14545. Epub 2025 Jan 5.

Abstract

With advances in long-read sequencing and assembly techniques, haplotype-resolved (phased) genome assemblies are becoming more common, also in the field of plant genomics. Computational tools to effectively explore these phased genomes, particularly for polyploid genomes, are currently limited. Here we describe a new strategy adopting a pangenome approach. To analyse both intra- and intergenomic variation in phased genome assemblies, we have made the software package PanTools ploidy-aware by updating the pangenome graph representation and adding several novel functionalities to assess synteny and gene retention, profile repeats and calculate synonymous and nonsynonymous mutation rates. Using PanTools, we constructed and analysed a pangenome comprising of one diploid and four tetraploid potato cultivars, and a pangenome of five diploid apple species. Both pangenomes show high intra- and intergenomic allelic diversity in terms of gene absence/presence, SNPs, indels and larger structural variants. Our findings show that the new functionalities and visualizations are useful to discover introgressions and detect likely misassemblies in phased genomes. PanTools is available at https://git.wur.nl/bioinformatics/pantools.

摘要

随着长读长测序和组装技术的进步,单倍型解析(定相)的基因组组装变得越来越普遍,在植物基因组学领域也是如此。目前,有效探索这些定相基因组的计算工具,尤其是针对多倍体基因组的工具,仍然有限。在此,我们描述了一种采用泛基因组方法的新策略。为了分析定相基因组组装中的基因组内和基因组间变异,我们通过更新泛基因组图谱表示并添加了几种新功能来评估共线性和基因保留、分析重复序列以及计算同义突变率和非同义突变率,从而使软件包PanTools能够感知倍性。使用PanTools,我们构建并分析了一个由一个二倍体和四个四倍体马铃薯品种组成的泛基因组,以及一个由五个二倍体苹果品种组成的泛基因组。这两个泛基因组在基因缺失/存在、单核苷酸多态性(SNP)、插入缺失和更大的结构变异方面均表现出较高的基因组内和基因组间等位基因多样性。我们的研究结果表明,新功能和可视化对于发现渐渗并检测定相基因组中可能的错误组装很有用。PanTools可在https://git.wur.nl/bioinformatics/pantools获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fdbb/11869183/8def0cee820b/PBI-23-874-g002.jpg

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