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MethylExtract: High-Quality methylation maps and SNV calling from whole genome bisulfite sequencing data

机译:甲基提取物:从全基因组亚硫酸氢盐测序数据获得的高质量甲基化图谱和SNV

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摘要

Whole genome methylation profiling at a single cytosine resolution is now feasible due to the advent of high-throughput sequencing techniques together with bisulfite treatment of the DNA. To obtain the methylation value of each individual cytosine, the bisulfite-treated sequence reads are first aligned to a reference genome, and then the profiling of the methylation levels is done from the alignments. A huge effort has been made to quickly and correctly align the reads and many different algorithms and programs to do this have been created. However, the second step is just as crucial and non-trivial, but much less attention has been paid to the final inference of the methylation states. Important error sources do exist, such as sequencing errors, bisulfite failure, clonal reads, and single nucleotide variants.We developed MethylExtract, a user friendly tool to: i) generate high quality, whole genome methylation maps and ii) detect sequence variation within the same sample preparation. The program is implemented into a single script and takes into account all major error sources. MethylExtract detects variation (SNVs – Single Nucleotide Variants) in a similar way to VarScan, a very sensitive method extensively used in SNV and genotype calling based on non-bisulfite-treated reads. The usefulness of MethylExtract is shown by means of extensive benchmarking based on artificial bisulfite-treated reads and a comparison to a recently published method, called Bis-SNP. MethylExtract is able to detect SNVs within High-Throughput Sequencing experiments of bisulfite treated DNA at the same time as it generates high quality methylation maps. This simultaneous detection of DNA methylation and sequence variation is crucial for many downstream analyses, for example when deciphering the impact of SNVs on differential methylation. An exclusive feature of MethylExtract, in comparison with existing software, is the possibility to assess the bisulfite failure in a statistical way. The source code, tutorial and artificial bisulfite datasets are available at and , and also permanently accessible from .
机译:由于高通量测序技术的出现以及DNA的亚硫酸氢盐处理,现在可以在单个胞嘧啶分辨率下进行全基因组甲基化分析。为了获得每个单个胞嘧啶的甲基化值,首先将亚硫酸氢盐处理的序列读数与参考基因组进行比对,然后从比对中进行甲基化水平的分析。为了快速正确地对齐读数,人们已经付出了巨大的努力,并且已经创建了许多不同的算法和程序来实现此目的。然而,第二步同样重要且重要,但是对甲基化状态的最终推断却少了很多注意。确实存在重要的错误来源,例如测序错误,亚硫酸氢盐失败,克隆读取和单核苷酸变异。我们开发了一种易于使用的工具MethylExtract,用于:i)生成高质量的全基因组甲基化图谱,以及ii)检测序列中的序列变异相同的样品制备。该程序在单个脚本中实施,并考虑了所有主要错误源。 MethylExtract以类似于VarScan的方式检测变异(SNV –单核苷酸变异体),这是一种非常敏感的方法,广泛用于SNV和基于未经亚硫酸氢盐处理的读数的基因型检测中。通过基于人工亚硫酸氢盐处理的读数的广泛基准测试以及与最近发布的称为Bis-SNP的方法的比较,表明了MethylExtract的有用性。 MethylExtract能够在亚硫酸氢盐处理的DNA的高通量测序实验中检测SNV,同时生成高质量的甲基化图谱。同时检测DNA甲基化和序列变异对于许多下游分析至关重要,例如,在破译SNV对差异甲基化的影响时。与现有软件相比,MethylExtract的一个独有功能是可以通过统计方式评估亚硫酸氢盐的失效。的源代码,教程和人工亚硫酸氢盐数据集可在和处获得,也可以从中永久访问。

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