Maptcha: an efficient parallel workflow for hybrid genome scaffolding.

IF 2.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS BMC Bioinformatics Pub Date : 2024-08-08 DOI:10.1186/s12859-024-05878-4
Oieswarya Bhowmik, Tazin Rahman, Ananth Kalyanaraman
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Abstract

Background: Genome assembly, which involves reconstructing a target genome, relies on scaffolding methods to organize and link partially assembled fragments. The rapid evolution of long read sequencing technologies toward more accurate long reads, coupled with the continued use of short read technologies, has created a unique need for hybrid assembly workflows. The construction of accurate genomic scaffolds in hybrid workflows is complicated due to scale, sequencing technology diversity (e.g., short vs. long reads, contigs or partial assemblies), and repetitive regions within a target genome.

Results: In this paper, we present a new parallel workflow for hybrid genome scaffolding that would allow combining pre-constructed partial assemblies with newly sequenced long reads toward an improved assembly. More specifically, the workflow, called Maptcha, is aimed at generating long scaffolds of a target genome, from two sets of input sequences-an already constructed partial assembly of contigs, and a set of newly sequenced long reads. Our scaffolding approach internally uses an alignment-free mapping step to build a contig,contig graph using long reads as linking information. Subsequently, this graph is used to generate scaffolds. We present and evaluate a graph-theoretic "wiring" heuristic to perform this scaffolding step. To enable efficient workload management in a parallel setting, we use a batching technique that partitions the scaffolding tasks so that the more expensive alignment-based assembly step at the end can be efficiently parallelized. This step also allows the use of any standalone assembler for generating the final scaffolds.

Conclusions: Our experiments with Maptcha on a variety of input genomes, and comparison against two state-of-the-art hybrid scaffolders demonstrate that Maptcha is able to generate longer and more accurate scaffolds substantially faster. In almost all cases, the scaffolds produced by Maptcha are at least an order of magnitude longer (in some cases two orders) than the scaffolds produced by state-of-the-art tools. Maptcha runs significantly faster too, reducing time-to-solution from hours to minutes for most input cases. We also performed a coverage experiment by varying the sequencing coverage depth for long reads, which demonstrated the potential of Maptcha to generate significantly longer scaffolds in low coverage settings ( 1 × - 10 × ).

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Maptcha:用于混合基因组支架构建的高效并行工作流程。
背景:基因组组装涉及目标基因组的重建,依赖于脚手架方法来组织和连接部分组装的片段。长读数测序技术朝着更精确的长读数方向快速发展,加上短读数技术的持续使用,对混合组装工作流程产生了独特的需求。由于规模、测序技术的多样性(如短读取与长读取、等位片段或部分组装)以及目标基因组中的重复区域,在混合工作流中构建精确的基因组支架非常复杂:在本文中,我们提出了一种新的混合基因组支架并行工作流程,它可以将预构建的部分组装与新测序的长读数结合起来,从而改进组装。更具体地说,这个名为 Maptcha 的工作流程旨在从两组输入序列--已构建的等位基因部分装配和一组新测序的长读数--生成目标基因组的长支架。我们的脚手架方法在内部使用免比对映射步骤,以长读数作为链接信息,构建一个⟨ contig,contig ⟩图。随后,利用该图生成支架。我们提出并评估了一种图论 "布线 "启发式来执行这一脚手架步骤。为了在并行环境中实现高效的工作量管理,我们采用了一种分批技术,将脚手架任务分批进行,这样就能有效地并行化最后耗资较大的基于配准的组装步骤。这一步骤还允许使用任何独立的装配器生成最终的脚手架:我们使用 Maptcha 对各种输入基因组进行了实验,并与两种最先进的混合支架器进行了比较,结果表明 Maptcha 能够以更快的速度生成更长、更精确的支架。几乎在所有情况下,Maptcha 生成的脚手架都比最先进工具生成的脚手架至少长一个数量级(在某些情况下长两个数量级)。Maptcha 的运行速度也明显更快,在大多数输入情况下,其解决问题的时间从几小时缩短到几分钟。我们还通过改变长读数的测序覆盖深度进行了覆盖率实验,结果表明 Maptcha 有潜力在低覆盖率设置(1 × - 10 ×)下生成更长的脚手架。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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