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一种具有近邻相互作用的核苷酸替换模型。

A nucleotide substitution model with nearest-neighbour interactions.

作者信息

Lunter Gerton, Hein Jotun

机构信息

Bioinformatics group, Department of Statistics, University of Oxford, Oxford, UK.

出版信息

Bioinformatics. 2004 Aug 4;20 Suppl 1:i216-23. doi: 10.1093/bioinformatics/bth901.

Abstract

MOTIVATION

It is well known that neighbouring nucleotides in DNA sequences do not mutate independently of each other. In this paper, we introduce a context-dependent substitution model and derive an algorithm to calculate the likelihood of sequences evolving under this model. We use this algorithm to estimate neighbour-dependent substitution rates, as well as rates for dinucleotide substitutions, using a Bayesian sampling procedure. The model is irreversible, giving an arrow to time, and allowing the position of the root between a pair of sequences to be inferred without using out-groups.

RESULTS

We applied the model upon aligned human-mouse non-coding data. Clear neighbour dependencies were observed, including 17-18-fold increased CpG to TpG/CpA rates compared with other substitutions. Root inference positioned the root halfway the mouse and human tips, suggesting an approximately clock-like behaviour of the irreversible part of the substitution process.

摘要

动机

众所周知,DNA序列中相邻的核苷酸不会相互独立地发生突变。在本文中,我们引入了一种上下文相关的替换模型,并推导了一种算法来计算在此模型下序列进化的似然性。我们使用该算法,通过贝叶斯抽样程序来估计邻位依赖的替换率以及二核苷酸替换率。该模型是不可逆的,给出了时间箭头,并且无需使用外类群就能推断一对序列之间根的位置。

结果

我们将该模型应用于比对后的人类 - 小鼠非编码数据。观察到了明显的邻位依赖性,包括与其他替换相比,从CpG到TpG/CpA的替换率增加了17 - 18倍。根的推断将根置于小鼠和人类末端的中间位置,这表明替换过程不可逆部分具有近似时钟般的行为。

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