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综合视图:多队列、多表型数据和荟萃分析的 SNP 关联结果的可视化和解释。

Synthesis-View: visualization and interpretation of SNP association results for multi-cohort, multi-phenotype data and meta-analysis.

机构信息

Center for Human Genetics Research, Vanderbilt University Medical Center, Nashville TN, USA.

出版信息

BioData Min. 2010 Dec 16;3:10. doi: 10.1186/1756-0381-3-10.

Abstract

BACKGROUND

Initial genome-wide association study (GWAS) discoveries are being further explored through the use of large cohorts across multiple and diverse populations involving meta-analyses within large consortia and networks. Many of the additional studies characterize less than 100 single nucleotide polymorphisms (SNPs), often include multiple and correlated phenotypic measurements, and can include data from multiple-sites, multiple-studies, as well as multiple race/ethnicities. New approaches for visualizing resultant data are necessary in order to fully interpret results and obtain a broad view of the trends between DNA variation and phenotypes, as well as provide information on specific SNP and phenotype relationships.

RESULTS

The Synthesis-View software tool was designed to visually synthesize the results of the aforementioned types of studies. Presented herein are multiple examples of the ways Synthesis-View can be used to report results from association studies of DNA variation and phenotypes, including the visual integration of p-values or other metrics of significance, allele frequencies, sample sizes, effect size, and direction of effect.

CONCLUSIONS

To truly allow a user to visually integrate multiple pieces of information typical of a genetic association study, innovative views are needed to integrate multiple pieces of information. As a result, we have created "Synthesis-View" software for the visualization of genotype-phenotype association data in multiple cohorts. Synthesis-View is freely available for non-commercial research institutions, for full details see https://chgr.mc.vanderbilt.edu/synthesisview.

摘要

背景

通过在大型联盟和网络中进行荟萃分析,利用多个不同人群中的大型队列,进一步探索了最初的全基因组关联研究(GWAS)发现。许多额外的研究描述了不到 100 个单核苷酸多态性(SNP),通常包含多个相关的表型测量,并且可以包含来自多个站点、多个研究以及多个种族/族裔的数据。为了全面解释结果并获得 DNA 变异与表型之间趋势的广泛视图,以及提供有关特定 SNP 和表型关系的信息,需要新的方法来可视化产生的数据。

结果

设计了 Synthesis-View 软件工具来直观地综合上述类型研究的结果。本文介绍了 Synthesis-View 可用于报告 DNA 变异和表型关联研究结果的多种方法,包括视觉整合 p 值或其他显着性度量、等位基因频率、样本大小、效应大小和效应方向。

结论

为了真正允许用户直观地整合遗传关联研究中典型的多组信息,需要创新的视图来整合多组信息。因此,我们创建了“合成视图”软件,用于可视化多个队列中的基因型-表型关联数据。Synthesis-View 可免费用于非商业研究机构,详情请访问 https://chgr.mc.vanderbilt.edu/synthesisview。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/471e/3012023/e741996669a4/1756-0381-3-10-1.jpg

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