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ShinyCore:一个用于基于单核苷酸多态性数据建立核心种质库的R/Shiny程序。

ShinyCore: An R/Shiny program for establishing core collection based on single nucleotide polymorphism data.

作者信息

Kim Steven, Kim Dong Sub, Moyle Hana, Heo Seong

机构信息

Department of Mathematics and Statistics, California State University, Monterey Bay, Seaside, USA.

Department of Horticulture, Kongju National University, Yesan, Korea.

出版信息

Plant Methods. 2023 Oct 11;19(1):106. doi: 10.1186/s13007-023-01084-0.

DOI:10.1186/s13007-023-01084-0
PMID:37821997
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10566191/
Abstract

BACKGROUND

Managing and investigating all available genetic resources are challenging. As an alternative, breeders and researchers use core collection-a representative subset of the entire collection. A good core is characterized by high genetic diversity and low repetitiveness. Among the several available software, GenoCore uses a coverage criterion that does not require computationally expensive distance-based metrics.

RESULTS

ShinyCore is a new method to select a core collection through two phases. The first phase uses the coverage criterion to quickly attain a fixed coverage, and the second phase uses a newly devised score (referred to as the rarity score) to further enhance diversity. It can attain a fixed coverage faster than a currently available algorithm devised for the coverage criterion, so it will benefit users who have big data. ShinyCore attains the minimum coverage specified by a user faster than GenoCore, and it then seeks to add entries with the rarest allele for each marker. Therefore, measures of genetic diversity and distance can be improved.

CONCLUSION

Although GenoCore is a fast algorithm, its implementation is difficult for those unfamiliar with R, ShinyCore can be easily implemented in Shiny with RStudio and an interactive web applet is available for those who are not familiar with programming languages.

摘要

背景

管理和研究所有可用的遗传资源具有挑战性。作为一种替代方法,育种者和研究人员使用核心种质——整个种质库的一个具有代表性的子集。一个好的核心种质的特点是遗传多样性高且重复性低。在几种可用的软件中,GenoCore使用一种覆盖标准,该标准不需要基于距离的计算成本高昂的度量。

结果

ShinyCore是一种通过两个阶段选择核心种质的新方法。第一阶段使用覆盖标准快速达到固定覆盖,第二阶段使用新设计的分数(称为稀有度分数)进一步提高多样性。它比目前为覆盖标准设计的算法更快地达到固定覆盖,因此将使拥有大数据的用户受益。ShinyCore比GenoCore更快地达到用户指定的最小覆盖,然后它会为每个标记寻找具有最稀有等位基因的条目。因此,可以提高遗传多样性和距离的度量。

结论

尽管GenoCore是一种快速算法,但对于不熟悉R的人来说,它的实施很困难,ShinyCore可以很容易地在RStudio的Shiny中实现,并且为不熟悉编程语言的人提供了一个交互式网络小程序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/f8cae41008ac/13007_2023_1084_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/0ca7be6eac3d/13007_2023_1084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/80807a7e5c40/13007_2023_1084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/969086b50528/13007_2023_1084_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/309876e15c48/13007_2023_1084_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/f8cae41008ac/13007_2023_1084_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/0ca7be6eac3d/13007_2023_1084_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/80807a7e5c40/13007_2023_1084_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/969086b50528/13007_2023_1084_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/309876e15c48/13007_2023_1084_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/66ed/10566191/f8cae41008ac/13007_2023_1084_Fig5_HTML.jpg

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本文引用的文献

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Comparison Between Core Set Selection Methods Using Different Illumina Marker Platforms: A Case Study of Assessment of Diversity in Wheat.使用不同Illumina标记平台的核心种质选择方法比较:以小麦多样性评估为例
Front Plant Sci. 2020 Jul 9;11:1040. doi: 10.3389/fpls.2020.01040. eCollection 2020.
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Core Hunter 3: flexible core subset selection.
Core Hunter 3:灵活的核心子集选择。
BMC Bioinformatics. 2018 May 31;19(1):203. doi: 10.1186/s12859-018-2209-z.
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GenoCore: A simple and fast algorithm for core subset selection from large genotype datasets.GenoCore:一种从大型基因型数据集中选择核心子集的简单快速算法。
PLoS One. 2017 Jul 20;12(7):e0181420. doi: 10.1371/journal.pone.0181420. eCollection 2017.
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Characterization of polyploid wheat genomic diversity using a high-density 90,000 single nucleotide polymorphism array.利用高密度90,000单核苷酸多态性阵列对多倍体小麦基因组多样性进行表征。
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