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Extending assembly of short DNA sequences to handle error

机译:扩展短DNA序列的装配以处理错误

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Inexpensive de novo genome sequencing, particularly in organisms with small genomes, is now possible using several new sequencing technologies. Some of these technologies such as that from Illumina's Solexa Sequencing, produce high genomic coverage by generating a very large number of small reads (~30 bp). While prior work shows that partial assembly can be performed by k-mer extension in error-free reads, this algorithm is unsuccessful with the sequencing error rates found in practice. We present VCAKE (Verified Consensus Assembly by K-mer Extension), a modification of simple k-mer extension that overcomes error by using high depth coverage. Though it is a simple modification of a previous approach, we show significant improvements in assembly results on simulated and experimental datasets that include error.
机译:现在,可以使用几种新的测序技术进行廉价的从头测序基因组测序,尤其是在基因组较小的生物中。其中的某些技术(例如,Illumina的Solexa测序技术)通过产生大量小读数(约30 bp)来产生高基因组覆盖率。尽管先前的工作表明可以通过k-mer扩展在无错误阅读中进行部分组装,但该算法在实践中发现的测序错误率不高。我们介绍了VCAKE(通过K-mer扩展程序验证的共识大会),这是对简单的K-mer扩展程序的修改,可通过使用高深度覆盖来克服错误。尽管它是对先前方法的简单修改,但是我们在包含错误的模拟和实验数据集上显示了装配结果的显着改进。

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