Zim4rv:一个R包建模零膨胀计数表型上基于区域的罕见变异。

IF 2.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS BMC Bioinformatics Pub Date : 2025-01-16 DOI:10.1186/s12859-024-06029-5
Xiaomin Liu, Yi-Ju Li, Qiao Fan
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引用次数: 0

摘要

背景:随着下一代测序技术的进步,各种基于基因的罕见变异关联检测已经开发出来,特别是针对二元和连续表型。相比之下,对于不遵循二项分布或正态分布的性状,可用的方法较少。为了解决这个问题,我们之前提出了一组基于负担和内核的稀有变体测试,用于遵循零膨胀泊松(ZIP)分布的计数数据,称为ZIP-b和ZIP-k测试。我们试图扩展方法以适应负二项分布,并在一个新的R包中实现这些测试。结果:我们引入了ZIM4rv,这是一个R软件包,旨在分析罕见变异与零膨胀计数结果的关联。我们的软件包提供了我们团队开发的两个新模型:我们之前提出的ZIP-b和ZIP-k测试,以及新导出的负二项负担和内核测试(ZINB-b, ZINB-k)。此外,我们还包括一个特设的两阶段分析,分别测试零和非零作为二进制结果和非零作为连续结果。为了展示我们平台的实用性,我们应用该程序分析来自ROSMAP队列的神经斑块计数数据。结论:R软件包ZIM4rv提供了一个集成的工作流程,用于对一组具有零膨胀计数数据的罕见变异进行关联测试。
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Zim4rv: an R package to modeling zero-inflated count phenotype on regional-based rare variants.

Background: With the advance of next-generation sequencing, various gene-based rare variant association tests have been developed, particularly for binary and continuous phenotypes. In contrast, fewer methods are available for traits not following binomial or normal distributions. To address this, we previously proposed a set of burden- and kernel-based rare variant tests for count data following zero-inflated Poisson (ZIP) distributions, referred to as ZIP-b and ZIP-k tests. We sought to extend the methods to accommodate negative binomial distribution and implemented these tests in a new R package.

Results: We introduce ZIM4rv, an R package designed to analyze the association of rare variants with zero-inflated counts outcomes. Our package offers two novel models developed by our team: our previously proposed ZIP-b and ZIP-k tests, and the newly derived Negative Binomial Burden and Kernel Test (ZINB-b, ZINB-k). Additionally, we include an ad-hoc two-stage analysis, testing zero and non-zero as a binary outcome and non-zero as a continuous outcome, respectively. To showcase the utility of our platform, we applied this program to analyze neuritic plaque count data from the ROSMAP cohort.

Conclusion: The R package ZIM4rv presents an integrated workflow for conducting association tests on a set of rare variants with zero-inflated counts data.

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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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