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基于标记点过程模型的定量基因组数据中任意长度差异表达区域的发现。

Finding differentially expressed regions of arbitrary length in quantitative genomic data based on marked point process model.

机构信息

Department of Statistics, the University of Warwick, Coventry CV4 7AL, UK.

出版信息

Bioinformatics. 2012 Sep 15;28(18):i633-i639. doi: 10.1093/bioinformatics/bts371.

Abstract

MOTIVATION

High-throughput nucleotide sequencing technologies provide large amounts of quantitative genomic data at nucleotide resolution, which are important for the present and future biomedical researches; for example differential analysis of base-level RNA expression data will improve our understanding of transcriptome, including both coding and non-coding genes. However, most studies of these data have relied on existing genome annotations and thus are limited to the analysis of known transcripts.

RESULTS

In this article, we propose a novel method based on a marked point process model to find differentially expressed genomic regions of arbitrary length without using genome annotations. The presented method conducts a statistical test for differential analysis in regions of various lengths at each nucleotide and searches the optimal configuration of the regions by using a Monte Carlo simulation. We applied the proposed method to both synthetic and real genomic data, and their results demonstrate the effectiveness of our method.

AVAILABILITY

The program used in this study is available at https://sites.google.com/site/hiroshihatsuda/.

CONTACT

H.Hatsuda@warwick.ac.uk.

摘要

动机

高通量核苷酸测序技术以核苷酸分辨率提供了大量定量基因组数据,这对当前和未来的生物医学研究非常重要;例如,对碱基水平 RNA 表达数据的差异分析将提高我们对转录组的理解,包括编码基因和非编码基因。然而,这些数据的大多数研究都依赖于现有的基因组注释,因此仅限于对已知转录本的分析。

结果

在本文中,我们提出了一种基于标记点过程模型的新方法,无需使用基因组注释即可找到任意长度的差异表达基因组区域。该方法在每个核苷酸处对不同长度的区域进行统计检验,并通过蒙特卡罗模拟搜索区域的最佳配置。我们将所提出的方法应用于合成和真实的基因组数据,其结果证明了我们方法的有效性。

可用性

本研究中使用的程序可在 https://sites.google.com/site/hiroshihatsuda/ 获得。

联系方式

H.Hatsuda@warwick.ac.uk

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b07d/3436798/02bb0379da1e/bts371f1.jpg

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