DISTREE:用于估计排列DNA序列之间的遗传距离的工具。

J Schäfer, M Schöniger
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引用次数: 4

摘要

动机:从比对的DNA数据中估计的替代率可以用作研究这些序列的系统发育关系的遗传距离。为此,必须假设一个最充分地描述这一过程的核苷酸替代的马尔可夫模型。结果:提出了一个程序,估计替代率及其标准误差的各种马尔可夫模型。Hasegawa et al. (J. Mol. evolution .)引入的模型。(22,160 -174, 1985)是唯一需要用数值方法计算距离和标准偏差的方法,因为无法推导出解析公式。每个模型以两种不同的变体实现:(i)假设速率同质性或(ii)从序列位点上的γ分布替代率开始。非均相取代率的估算基于Tamura和Nei (Mol. Biol)提出的方法。另一个星球。, 10, 512-526, 1993)。所有必需的参数都是从序列数据中估计出来的,因此不要求用户提供任何额外的输入。该程序的一个目标是支持用户选择最充分地描述给定数据集演变的特定模型。为此,提供了对该模型拟合的更详细的分析。利用邻居连接算法从推断的距离重建系统发育树也是可行的。
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DISTREE: a tool for estimating genetic distances between aligned DNA sequences.

Motivation: Substitution rates estimated from aligned DNA data can be used as genetic distances to investigate the phylogenetic relationship of those sequences. For this purpose, a Markov model of nucleotide substitution has to be assumed that describes this process most adequately.

Results: A program is presented that estimates substitution rates and their standard errors for a variety of Markov models. The model introduced by Hasegawa et al. (J. Mol. Evol., 22, 160-174, 1985) is the only one for which distances and standard deviations need to be calculated numerically, since analytical formulae cannot be derived. Each model is implemented in two different variants: (i) assuming rate homogeneity or (ii) starting from Gamma-distributed substitution rates across sequence sites. The estimation of heterogeneous substitution rates is based on a method suggested by Tamura and Nei (Mol. Biol. Evol., 10, 512-526, 1993). All required parameters are estimated from sequence data, hence the user is not asked to supply any additional input. One goal of the program is to support the user when choosing a particular model that describes most adequately the evolution of the given data set. For this purpose, a more detailed analysis of this model fit is provided. Phylogenetic trees reconstructed from the inferred distances using the neighbor-joining algorithm are also available.

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A genetic algorithm for multiple molecular sequence alignment. Displaying the information contents of structural RNA alignments: the structure logos. Q-RT-PCR: data analysis software for measurement of gene expression by competitive RT-PCR. SS3D-P2: a three dimensional substructure search program for protein motifs based on secondary structure elements. XDOM, a graphical tool to analyse domain arrangements in any set of protein sequences.
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