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人类基因组中突变率的变化有多少是可以解释的?

How much of the variation in the mutation rate along the human genome can be explained?

作者信息

Eyre-Walker Adam, Eyre-Walker Ying Chen

机构信息

School of Life Sciences, University of Sussex, Brighton, BN1 9QG, United Kingdom

School of Life Sciences, University of Sussex, Brighton, BN1 9QG, United Kingdom.

出版信息

G3 (Bethesda). 2014 Jul 3;4(9):1667-70. doi: 10.1534/g3.114.012849.

Abstract

It has been claimed recently that it may be possible to predict the rate of de novo mutation of each site in the human genome with a high degree of accuracy [Michaelson et al. (2012), Cell 151: 1431-1442]. We show that this claim is unwarranted. By considering the correlation between the rate of de novo mutation and the predictions from the model of Michaelson et al., we show there could be substantial unexplained variance in the mutation rate. We investigate whether the model of Michaelson et al. captures variation at the single nucleotide level that is not due to simple context. We show that the model captures a substantial fraction of this variation at CpG dinucleotides but fails to explain much of the variation at non-CpG sites.

摘要

最近有人声称,有可能以高度的准确性预测人类基因组中每个位点的新生突变率[迈克尔森等人(2012年),《细胞》151卷:1431 - 1442页]。我们表明这一说法是没有根据的。通过考虑新生突变率与迈克尔森等人模型的预测之间的相关性,我们表明突变率可能存在大量无法解释的变异。我们研究了迈克尔森等人的模型是否捕捉到了并非由于简单上下文引起的单核苷酸水平的变异。我们表明该模型捕捉到了CpG二核苷酸处这种变异的很大一部分,但未能解释非CpG位点的大部分变异。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65a7/4169158/764b91dd514f/1667f1.jpg

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