首页> 美国卫生研究院文献>BMC Genomics >BALLI: Bartlett-adjusted likelihood-based linear model approach for identifying differentially expressed genes with RNA-seq data
【2h】

BALLI: Bartlett-adjusted likelihood-based linear model approach for identifying differentially expressed genes with RNA-seq data

机译:BALLI:Bartlett调整的基于似然性的线性模型方法用于利用RNA-seq数据鉴定差异表达的基因

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

BackgroundTranscriptomic profiles can improve our understanding of the phenotypic molecular basis of biological research, and many statistical methods have been proposed to identify differentially expressed genes (DEGs) under two or more conditions with RNA-seq data. However, statistical analyses with RNA-seq data are often limited by small sample sizes, and global variance estimates of RNA expression levels have been utilized as prior distributions for gene-specific variance estimates, making it difficult to generalize the methods to more complicated settings. We herein proposed a Bartlett-Adjusted Likelihood-based LInear mixed model approach (BALLI) to analyze more complicated RNA-seq data. The proposed method estimates the technical and biological variances with a linear mixed-effects model, with and without adjusting small sample bias using Bartlkett’s corrections.
机译:背景转录组概况可以提高我们对生物学研究的表型分子基础的了解,并且已经提出了许多统计方法来鉴定在两个或更多条件下具有RNA序列数据的差异表达基因(DEG)。但是,使用RNA-seq数据进行的统计分析通常受到小样本量的限制,并且RNA表达水平的总体差异估计已被用作基因特异性差异估计的先验分布,从而难以将方法推广到更复杂的设置。我们在此提出了一种基于Bartlett调整似然法的LInear混合模型方法(BALLI),以分析更复杂的RNA-seq数据。所提出的方法使用线性混合效应模型估算技术和生物学差异,并且可以使用Bartlkett校正来调整和不调整小的样本偏差。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号