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BayesCall: A model-based base-calling algorithm for high-throughput short-read sequencing

机译:BayesCall:高通量短读测序的基于模型的碱基检出算法

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摘要

Extracting sequence information from raw images of fluorescence is the foundation underlying several high-throughput sequencing platforms. Some of the main challenges associated with this technology include reducing the error rate, assigning accurate base-specific quality scores, and reducing the cost of sequencing by increasing the throughput per run. To demonstrate how computational advancement can help to meet these challenges, a novel model-based base-calling algorithm, BayesCall, is introduced for the Illumina sequencing platform. Being founded on the tools of statistical learning, BayesCall is flexible enough to incorporate various features of the sequencing process. In particular, it can easily incorporate time-dependent parameters and model residual effects. This new approach significantly improves the accuracy over Illumina's base-caller Bustard, particularly in the later cycles of a sequencing run. For 76-cycle data on a standard viral sample, phiX174, BayesCall improves Bustard's average per-base error rate by ∼51%. The probability of observing each base can be readily computed in BayesCall, and this probability can be transformed into a useful base-specific quality score with a high discrimination ability. A detailed study of BayesCall's performance is presented here.
机译:从荧光的原始图像中提取序列信息是几个高通量测序平台的基础。与该技术相关的一些主要挑战包括降低错误率,分配准确的特定于碱基的质量得分以及通过提高每次运行的通量来降低测序成本。为了演示计算的进步如何帮助应对这些挑战,针对Illumina测序平台引入了一种基于模型的新颖碱基调用算法BayesCall。 BayesCall建立在统计学习工具的基础之上,具有足够的灵活性,可以整合测序过程的各种功能。特别是,它可以轻松地合并与时间有关的参数并为残差模型建模。这种新方法大大提高了Illumina基本调用程序Bustard的准确性,尤其是在测序运行的后期循环中。对于标准病毒样品phiX174上的76个周期的数据,BayesCall将Bustard的平均碱基错误率提高了约51%。可以在BayesCall中轻松计算观察每个碱基的概率,并且可以将该概率转换为具有高判别能力的有用的特定于碱基的质量得分。此处详细介绍了BayesCall的性能。

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