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PRECISION.seq:一个用于对微小RNA测序中的深度归一化进行基准测试的R软件包。

PRECISION.seq: An R Package for Benchmarking Depth Normalization in microRNA Sequencing.

作者信息

Zou Jian, Düren Yannick, Qin Li-Xuan

机构信息

Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, United States.

Department of Mathematics, Ruhr-University Bochum, Bochum, Germany.

出版信息

Front Genet. 2022 Jan 28;12:823431. doi: 10.3389/fgene.2021.823431. eCollection 2021.

DOI:10.3389/fgene.2021.823431
PMID:35154266
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8832140/
Abstract

We present a new R package for assessing the performance of depth normalization in microRNA sequencing data. It provides a pair of microRNA sequencing data sets for the same set of tumor samples, additional pairs of data sets simulated by re-sampling under various patterns of differential expression, and a collection of numerical and graphical tools for assessing the performance of normalization methods. Users can easily assess their chosen normalization method and compare its performance to nine methods already included in the package. enables an objective and systematic evaluation of normalization methods in microRNA sequencing using realistically distributed and robustly benchmarked data under a wide range of differential expression patterns. To our best knowledge, this is the first such tool available. The data sets and source code of the R package can be found at https://github.com/LXQin/PRECISION.seq.

摘要

我们展示了一个用于评估微小RNA测序数据中深度归一化性能的新R包。它为同一组肿瘤样本提供了一对微小RNA测序数据集,通过在各种差异表达模式下重新采样模拟的额外数据集对,以及一组用于评估归一化方法性能的数值和图形工具。用户可以轻松评估他们选择的归一化方法,并将其性能与该包中已包含的九种方法进行比较。这使得能够在广泛的差异表达模式下,使用实际分布且经过严格基准测试的数据,对微小RNA测序中的归一化方法进行客观和系统的评估。据我们所知,这是首个此类可用工具。该R包的数据集和源代码可在https://github.com/LXQin/PRECISION.seq上找到。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/a253423e901a/fgene-12-823431-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/6838c173c26d/fgene-12-823431-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/9be8f83598df/fgene-12-823431-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/a253423e901a/fgene-12-823431-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/6838c173c26d/fgene-12-823431-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/9be8f83598df/fgene-12-823431-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4337/8832140/a253423e901a/fgene-12-823431-g003.jpg

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本文引用的文献

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RLE plots: Visualizing unwanted variation in high dimensional data.RLE图:可视化高维数据中的不必要变异。
PLoS One. 2018 Feb 5;13(2):e0191629. doi: 10.1371/journal.pone.0191629. eCollection 2018.
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Comparison of normalization methods for differential gene expression analysis in RNA-Seq experiments: A matter of relative size of studied transcriptomes.
辣椒果实颜色的遗传图谱:四个栽培种的比较分析。
Theor Appl Genet. 2024 May 14;137(6):130. doi: 10.1007/s00122-024-04635-8.
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Genome Biol. 2014 Feb 3;15(2):R29. doi: 10.1186/gb-2014-15-2-r29.
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Brief Bioinform. 2013 Nov;14(6):671-83. doi: 10.1093/bib/bbs046. Epub 2012 Sep 17.
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