Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data.

Calculation of Tajima's D and other neutrality test statistics from low depth next-generation sequencing data.
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DOI:
10.1186/1471-2105-14-289
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发表时间:
2013-10-02
期刊:
影响因子:
3
通讯作者:
Nielsen R
Nielsen R
中科院分区:
生物学4区
文献类型:
--
作者:
Korneliussen TS;Moltke I;Albrechtsen A;Nielsen R

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许多不同的统计数据被用于检测自然选择使用DNA测序数据,包括统计,是频谱的总结,如田岛的D。这些统计数据现在经常被应用于下一代测序(NGS)数据的分析。然而,从NGS数据的频谱的估计受到低测序覆盖率的强烈影响;测序深度的固有技术依赖性变化导致基因组区域之间的统计值的系统差异。我们已经开发出一种方法,可容纳的不确定性的数据时,计算站点频率为基础的中立性测试统计。该方法的显著特征在于,它隐含地解决了不同测序深度、缺失数据的问题,并且避免了推断用于分析的可变位点的需要,从而避免了由SNP发现过程引入的确定问题。使用经验贝叶斯方法进行快速计算,我们表明,这种方法产生的结果低覆盖率NGS数据相比,当基因型是已知的,没有不确定性。我们还验证了1000个基因组项目的数据分析的方法。该方法在一个快速框架中实现,使研究人员能够在全基因组范围内进行这些中性测试。
A number of different statistics are used for detecting natural selection using DNA sequencing data, including statistics that are summaries of the frequency spectrum, such as Tajima’s D. These statistics are now often being applied in the analysis of Next Generation Sequencing (NGS) data. However, estimates of frequency spectra from NGS data are strongly affected by low sequencing coverage; the inherent technology dependent variation in sequencing depth causes systematic differences in the value of the statistic among genomic regions. We have developed an approach that accommodates the uncertainty of the data when calculating site frequency based neutrality test statistics. A salient feature of this approach is that it implicitly solves the problems of varying sequencing depth, missing data and avoids the need to infer variable sites for the analysis and thereby avoids ascertainment problems introduced by a SNP discovery process. Using an empirical Bayes approach for fast computations, we show that this method produces results for low-coverage NGS data comparable to those achieved when the genotypes are known without uncertainty. We also validate the method in an analysis of data from the 1000 genomes project. The method is implemented in a fast framework which enables researchers to perform these neutrality tests on a genome-wide scale.
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