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Systematic exploration of error sources in pyrosequencing flowgram data

机译:系统分析焦磷酸测序流程图数据中的误差源

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Motivation: 454 pyrosequencing, by Roche Diagnostics, has emerged as an alternative to Sanger sequencing when it comes to read lengths, performance and cost, but shows higher per-base error rates. Although there are several tools available for noise removal, targeting different application fields, data interpretation would benefit from a better understanding of the different error types.Results: By exploring 454 raw data, we quantify to what extent different factors account for sequencing errors. In addition to the well-known homopolymer length inaccuracies, we have identified errors likely to originate from other stages of the sequencing process. We use our findings to extend the flowsim pipeline with functionalities to simulate these errors, and thus enable a more realistic simulation of 454 pyrosequencing data with flowsim.
机译:动机:在读取长度,性能和成本方面,罗氏诊断公司(Roche Diagnostics)的454焦磷酸测序已成为Sanger测序的替代方法,但显示出更高的每碱基错误率。尽管有多种噪声消除工具可用于不同的应用领域,但通过更好地理解不同的错误类型,数据解释将受益。结果:通过研究454个原始数据,我们可以量化不同因素在多大程度上造成了顺序错误。除了众所周知的均聚物长度错误外,我们还确定了可能源自测序过程其他阶段的错误。我们使用我们的发现来扩展具有功能的flowsim管道,以模拟这些错误,从而使使用flowsim对454个焦磷酸测序数据进行更真实的模拟。

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