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Poisson adjacency distributions in genome comparison: multichromosomal, circular, signed and unsigned cases.

机译:基因组比较中的泊松邻接分布:多染色体,圆形,有符号和无符号案例。

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摘要

The number of common adjacencies of genetic markers, as a measure of the similarity of two genomes, has been widely used as indicator of evolutionary relatedness and as the basis for inferring phylogenetic relationships. Its probability distribution enables statistical tests in detecting whether significant evolutionary signal remains in the marker order. In this article, we derive the probability distributions of the number of adjacencies for a number of types of genome--signed or unsigned, circular or linear, single-chromosome or multichromosomal. Generating functions are found for singlechromosome cases, from which exact counts can be calculated. Probability approaches are adopted for multichromosomal cases, where we.nd the exact values for expectations and variances. In both cases, the limiting distributions are derived in term of numbers of adjacencies. For all unsigned cases, the limiting distribution is Poisson with parameter 2; for all signed cases, the limiting distribution is Poisson with parameter (1/2).
机译:作为两个基因组相似性的量度,遗传标记的常见邻接数已广泛用作进化相关性的指标和推断系统发生关系的基础。它的概率分布使统计测试能够检测出重要的进化信号是否仍按标记顺序排列。在本文中,我们得出了许多类型的基因组-有符号或无符号,圆形或线性,单染色体或多染色体的邻接数的概率分布。找到了用于单染色体情况的生成函数,可以从中计算出精确的计数。对于多染色体情况,采用了概率方法,在其中我们找到了期望值和方差的确切值。在两种情况下,极限分布都是根据邻接数得出的。对于所有未签名的情况,极限分布为参数2的泊松。对于所有有符号的情况,极限分布为带参数(1/2)的泊松。

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