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An efficient approach to BAC based assembly of complex genomes

机译:基于BAC的复杂基因组组装的有效方法

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Background There has been an exponential growth in the number of genome sequencing projects since the introduction of next generation DNA sequencing technologies. Genome projects have increasingly involved assembly of whole genome data which produces inferior assemblies compared to traditional Sanger sequencing of genomic fragments cloned into bacterial artificial chromosomes (BACs). While whole genome shotgun sequencing using next generation sequencing (NGS) is relatively fast and inexpensive, this method is extremely challenging for highly complex genomes, where polyploidy or high repeat content confounds accurate assembly, or where a highly accurate ‘gold’ reference is required. Several attempts have been made to improve genome sequencing approaches by incorporating NGS methods, to variable success. Results We present the application of a novel BAC sequencing approach which combines indexed pools of BACs, Illumina paired read sequencing, a sequence assembler specifically designed for complex BAC assembly, and a custom bioinformatics pipeline. We demonstrate this method by sequencing and assembling BAC cloned fragments from bread wheat and sugarcane genomes. Conclusions We demonstrate that our assembly approach is accurate, robust, cost effective and scalable, with applications for complete genome sequencing in large and complex genomes.
机译:背景技术自从引入下一代DNA测序技术以来,基因组测序项目的数量呈指数增长。与传统的克隆到细菌人工染色体(BAC)中的基因组片段的Sanger测序相比,基因组项目越来越多地涉及对全基因组数据的组装,从而产生劣等的组装。尽管使用下一代测序(NGS)进行全基因组shot弹枪测序相对快速且便宜,但对于高度复杂的基因组(多倍体或高重复含量混淆了准确的组装,或需要高度准确的“金”参比),此方法极具挑战性。为了结合成功,人们已经进行了一些尝试,通过结合NGS方法来改善基因组测序方法。结果我们介绍了一种新颖的BAC测序方法的应用,该方法结合了BAC的索引库,Illumina配对读取测序,专为复杂BAC组装而设计的序列组装器和定制的生物信息学流水线。我们通过测序和组装面包小麦和甘蔗基因组的BAC克隆片段来证明此方法。结论我们证明了我们的组装方法准确,可靠,具有成本效益和可扩展性,可用于大型和复杂基因组的完整基因组测序。

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