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Hierarchical genome assembly method using single long insert library

机译:使用单个长插入文库的分级基因组组装方法

摘要

The present invention is generally directed to a hierarchical genome assembly process for producing high-quality de novo genome assemblies. The method utilizes a single, long-insert, shotgun DNA library in conjunction with Single Molecule, Real-Time (SMRT®) DNA sequencing, and obviates the need for additional sample preparation and sequencing data sets required for previously described hybrid assembly strategies. Efficient de novo assembly from genomic DNA to a finished genome sequence is demonstrated for several microorganisms using as little as three SMRT® cells, and for bacterial artificial chromosomes (BACs) using sequencing data from just one SMRT® Cell. Part of this new assembly workflow is a new consensus algorithm which takes advantage of SMRT® sequencing primary quality values, to produce a highly accurate de novo genome sequence, exceeding 99.999% (QV 50) accuracy. The methods are typically performed on a computer and comprise an algorithm that constructs sequence alignment graphs from pairwise alignment of sequence reads to a common reference.
机译:本发明总体上涉及用于产生高质量的从头基因组组装体的分级基因组组装方法。该方法结合了单分子实时(SMRT®)DNA测序技术,利用了一个长插入的conjunction弹枪DNA库,从而消除了先前描述的混合装配策略所需的其他样品制备和测序数据集的需要。仅使用三个SMRT®细胞,就可以对几种微生物进行高效的从头组装,而仅使用一个SMRT®Cell的测序数据就可以对细菌人工染色体(BAC)进行高效的从头组装。这种新装配流程的一部分是一种新的共识算法,该算法利用SMRT®测序的原始质量值来产生高度准确的从头基因组序列,其准确性超过99.999%(QV 50)。该方法通常在计算机上执行,并且包括一种算法,该算法从序列读取到公共参考的成对比对构建序列比对图。

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