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UMI-tools: Modelling sequencing errors in Unique Molecular Identifiers to improve quantification accuracy.

机译:UMI工具:对唯一分子标识符中的测序错误进行建模,以提高定量准确性。

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摘要

Unique Molecular Identifiers (UMIs) are random oligonucleotide barcodes that are increasingly used in high-throughput sequencing experiments. Through a UMI, identical copies arising from distinct molecules can be distinguished from those arising through PCR-amplification of the same molecule. However, bioinformatic methods to leverage the information from UMIs have yet to be formalised. In particular, sequencing errors in the UMI sequence are often ignored, or else resolved in an ad-hoc manner. We show that errors in the UMI sequence are common and introduce network based methods to account for these errors when identifying PCR duplicates. Using these methods, we demonstrate improved quantification accuracy both under simulated conditions and real iCLIP and single cell RNA-Seq datasets. Reproducibility between iCLIP replicates and single cell RNA Seq clustering are both improved using our proposed network-based method, demonstrating the value of properly accounting for errors in UMIs. These methods are implemented in the open source UMI-tools software package.
机译:独特的分子标识符(UMI)是随机的寡核苷酸条形码,在高通量测序实验中越来越多地使用。通过UMI,可以将源自不同分子的相同拷贝与通过相同分子的PCR扩增产生的拷贝区分开。但是,利用UMI信息的生物信息学方法尚未正式化。特别是,通常会忽略或以特殊方式解决UMI序列中的排序错误。我们证明了UMI序列中的错误很常见,并介绍了基于网络的方法来在识别PCR重复项时解决这些错误。使用这些方法,我们证明了在模拟条件下以及真实的iCLIP和单细胞RNA-Seq数据集下提高的定量准确性。使用我们提出的基于网络的方法,iCLIP复制和单细胞RNA Seq聚类之间的可重复性都得到了改善,证明了正确考虑UMI错误的价值。这些方法在开源UMI工具软件包中实现。

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