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A comprehensive literature review of haplotyping software and methods for use with unrelated individuals

机译:有关不相关个人使用的单元型软件和方法的全面文献综述

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摘要

Interest in the assignment and frequency analysis of haplotypes in samples of unrelated individuals has increased immeasurably as a result of the emphasis placed on haplotype analyses by, for example, the International HapMap Project and related initiatives. Although there are many available computer programs for haplotype analysis applicable to samples of unrelated individuals, many of these programs have limitations and/or very specific uses. In this paper, the key features of available haplotype analysis software for use with unrelated individuals, as well as pooled DNA samples from unrelated individuals, are summarised. Programs for haplotype analysis were identified through keyword searches on PUBMED and various internet search engines, a review of citations from retrieved papers and personal communications, up to June 2004. Priority was given to functioning computer programs, rather than theoretical models and methods. The available software was considered in light of a number of factors: the algorithm(s) used, algorithm accuracy, assumptions, the accommodation of genotyping error, implementation of hypothesis testing, handling of missing data, software characteristics and web-based implementations. Review papers comparing specific methods and programs are also summarised. Forty-six haplotyping programs were identified and reviewed. The programs were divided into two groups: those designed for individual genotype data (a total of 43 programs) and those designed for use with pooled DNA samples (a total of three programs). The accuracy of programs using various criteria are assessed and the programs are categorised and discussed in light of: algorithm and method, accuracy, assumptions, genotyping error, hypothesis testing, missing data, software characteristics and web implementation. Many available programs have limitations (eg some cannot accommodate missing data) and/or are designed with specific tasks in mind (eg estimating haplotype frequencies rather than assigning most likely haplotypes to individuals). It is concluded that the selection of an appropriate haplotyping program for analysis purposes should be guided by what is known about the accuracy of estimation, as well as by the limitations and assumptions built into a program.
机译:由于国际HapMap项目和相关倡议对单倍型分析的重视,对无亲属个体样本中单倍型的分配和频率分析的兴趣显着增加。尽管有许多可用的用于单倍型分析的计算机程序适用于无关个体的样本,但是这些程序中有许多都有局限性和/或非常特定的用途。在本文中,总结了可用的单倍型分析软件的主要功能,这些软件可用于无关的个体,以及来自无关的个体的合并DNA样本。截至2004年6月,通过在PUBMED和各种互联网搜索引擎上进行关键字搜索,对检索到的论文和个人通讯的引用进行了审查,确定了用于单倍型分析的程序。优先考虑可运行的计算机程序,而不是理论模型和方法。考虑了以下因素来考虑可用的软件:使用的算法,算法的准确性,假设,基因分型错误的适应性,假设检验的实现,缺失数据的处理,软件特性和基于Web的实现。还总结了比较特定方法和程序的评论文件。确定并审查了46个单元型计划。这些程序分为两组:针对单个基因型数据设计的程序(总共43个程序)和针对合并的DNA样本设计的程序(总共3个程序)。使用各种标准评估程序的准确性,并根据以下算法对程序进行分类和讨论:算法和方法,准确性,假设,基因分型错误,假设检验,数据丢失,软件特性和Web实现。许多可用程序都有局限性(例如,某些程序无法容纳丢失的数据)和/或在设计时考虑了特定任务(例如,估计单倍型频率,而不是将最可能的单倍型分配给个人)。结论是,应根据对估计准确性的了解以及程序中的局限性和假设,指导为分析目的选择合适的单体型程序。

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