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本文引用的文献

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Sample size calculation based on generalized linear models for differential expression analysis in RNA-seq data.基于广义线性模型的RNA测序数据差异表达分析的样本量计算
Stat Appl Genet Mol Biol. 2016 Dec 1;15(6):491-505. doi: 10.1515/sagmb-2016-0008.
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PERMANOVA-S: association test for microbial community composition that accommodates confounders and multiple distances.PERMANOVA-S:用于微生物群落组成的关联测试,可处理混杂因素和多种距离。
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Practicability of detecting somatic point mutation from RNA high throughput sequencing data.从RNA高通量测序数据中检测体细胞点突变的可行性
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Sample size calculation while controlling false discovery rate for differential expression analysis with RNA-sequencing experiments.在RNA测序实验的差异表达分析中控制错误发现率时的样本量计算。
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On Sample Size and Power Calculation for Variant Set-Based Association Tests.基于变异集的关联检验的样本量与效能计算
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Systematic pan-cancer analysis of tumour purity.肿瘤纯度的系统性泛癌分析。
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SPS: A Simulation Tool for Calculating Power of Set-Based Genetic Association Tests.SPS:一种用于计算基于集合的基因关联测试效能的模拟工具。
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Power and sample-size estimation for microbiome studies using pairwise distances and PERMANOVA.使用成对距离和PERMANOVA进行微生物组研究的功效和样本量估计。
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Identification of active transcriptional regulatory elements from GRO-seq data.从基因表达连续性分析(GRO-seq)数据中鉴定活性转录调控元件
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Rare variant association studies: considerations, challenges and opportunities.罕见变异关联研究:考量、挑战与机遇
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基于高通量测序的实验的功效和样本量计算。

Power and sample size calculations for high-throughput sequencing-based experiments.

机构信息

Department of Statistics, National Cheng Kung University in Taiwan.

Department of Molecular Physiology and Biophysics, Vanderbilt University, USA.

出版信息

Brief Bioinform. 2018 Nov 27;19(6):1247-1255. doi: 10.1093/bib/bbx061.

DOI:10.1093/bib/bbx061
PMID:28605403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6291796/
Abstract

Power/sample size (power) analysis estimates the likelihood of successfully finding the statistical significance in a data set. There has been a growing recognition of the importance of power analysis in the proper design of experiments. Power analysis is complex, yet necessary for the success of large studies. It is important to design a study that produces statistically accurate and reliable results. Power computation methods have been well established for both microarray-based gene expression studies and genotyping microarray-based genome-wide association studies. High-throughput sequencing (HTS) has greatly enhanced our ability to conduct biomedical studies at the highest possible resolution (per nucleotide). However, the complexity of power computations is much greater for sequencing data than for the simpler genotyping array data. Research on methods of power computations for HTS-based studies has been recently conducted but is not yet well known or widely used. In this article, we describe the power computation methods that are currently available for a range of HTS-based studies, including DNA sequencing, RNA-sequencing, microbiome sequencing and chromatin immunoprecipitation sequencing. Most importantly, we review the methods of power analysis for several types of sequencing data and guide the reader to the relevant methods for each data type.

摘要

功效/样本量(功效)分析估计在数据集成功发现统计显著性的可能性。人们越来越认识到在实验的正确设计中进行功效分析的重要性。功效分析虽然复杂,但对于大型研究的成功却是必要的。设计出能够产生准确可靠结果的研究是很重要的。微阵列基因表达研究和基于基因分型的全基因组关联研究的功效计算方法已经得到很好的确立。高通量测序(HTS)大大提高了我们在尽可能高的分辨率(每个核苷酸)下进行生物医学研究的能力。然而,测序数据的功效计算复杂性比简单的基因分型阵列数据要大得多。最近已经对基于 HTS 的研究的功效计算方法进行了研究,但尚未广为人知或广泛使用。在本文中,我们描述了目前可用于一系列基于 HTS 的研究的功效计算方法,包括 DNA 测序、RNA 测序、微生物组测序和染色质免疫沉淀测序。最重要的是,我们回顾了几种测序数据的功效分析方法,并为每种数据类型引导读者了解相关方法。