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Opera: Reconstructing Optimal Genomic Scaffolds with High-Throughput Paired-End Sequences

机译:Opera:用高通量配对末端序列重建最佳基因组支架。

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Scaffolding, the problem of ordering and orienting contigs, typically using paired-end reads, is a crucial step in the assembly of high-quality draft genomes. Even as sequencing technologies and mate-pair protocols have improved significantly, scaffolding programs still rely on heuristics, with no gaurantees on the quality of the solution. In this work we explored the feasibility of an exact solution for scaffolding and present a first fixed-parameter tractable solution for assembly (Opera). We also describe a graph contraction procedure that allows the solution to scale to large scaffolding problems and demonstrate this by scaffolding several large real and synthetic datasets. In comparisons with existing scaffold-ers, Opera simultaneously produced longer and more accurate scaffolds demonstrating the utility of an exact approach. Opera also incorporates an exact quadratic programming formulation to precisely compute gap sizes.
机译:脚手架是重叠群的有序排列和定向问题,通常使用配对末端读取,是组装高质量草图基因组的关键步骤。即使测序技术和伴侣对协议有了显着改善,脚手架程序仍然依靠启发式方法,而对解决方案的质量没有任何保证。在这项工作中,我们探索了一种精确的脚手架解决方案的可行性,并提出了第一个固定参数固定式易组装解决方案(Opera)。我们还描述了一种图形收缩程序,该程序可使解决方案扩展到大型脚手架问题,并通过脚手架上几个大型的实际和综合数据集来演示这一问题。与现有的脚手架相比,Opera同时生产了更长,更准确的脚手架,证明了一种精确方法的实用性。 Opera还采用精确的二次编程公式来精确计算间隙大小。

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