BioVLAB-MMIA-NGS: microRNA-mRNA integrated analysis using high-throughput sequencing data

被引:25
作者
Chae, Heejoon [1 ]
Rhee, Sungmin [2 ]
Nephew, Kenneth P. [3 ]
Kim, Sun [2 ]
机构
[1] Indiana Univ, Sch Informat & Comp, Dept Comp Sci, Bloomington, IN 47404 USA
[2] Seoul Natl Univ, Sch Comp Sci & Engn, Seoul, South Korea
[3] Indiana Univ Sch Med, Indianapolis, IN 46202 USA
基金
新加坡国家研究基金会;
关键词
GENES; TOOL;
D O I
10.1093/bioinformatics/btu614
中图分类号
Q5 [生物化学];
学科分类号
070307 [化学生物学];
摘要
Motivation: It is now well established that microRNAs (miRNAs) play a critical role in regulating gene expression in a sequence-specific manner, and genome-wide efforts are underway to predict known and novel miRNA targets. However, the integrated miRNA-mRNA analysis remains a major computational challenge, requiring powerful informatics systems and bioinformatics expertise. Results: The objective of this study was to modify our widely recognized Web server for the integrated mRNA-miRNA analysis (MMIA) and its subsequent deployment on the Amazon cloud (BioVLAB-MMIA) to be compatible with high-throughput platforms, including next-generation sequencing (NGS) data (e.g. RNA-seq). We developed a new version called the BioVLAB-MMIA-NGS, deployed on both Amazon cloud and on a high-performance publicly available server called MAHA. By using NGS data and integrating various bioinformatics tools and databases, BioVLAB-MMIA-NGS offers several advantages. First, sequencing data is more accurate than array-based methods for determining miRNA expression levels. Second, potential novel miRNAs can be detected by using various computational methods for characterizing miRNAs. Third, because miRNA-mediated gene regulation is due to hybridization of an miRNA to its target mRNA, sequencing data can be used to identify many-to-many relationship between miRNAs and target genes with high accuracy.
引用
收藏
页码:265 / 267
页数:3
相关论文
共 20 条
[1]
The DIANA-mirExTra Web Server: From Gene Expression Data to MicroRNA Function [J].
Alexiou, Panagiotis ;
Maragkakis, Manolis ;
Papadopoulos, Giorgio L. ;
Simmosis, Victor A. ;
Zhang, Lin ;
Hatzigeorgiou, Artemis G. .
PLOS ONE, 2010, 5 (02)
[2]
Differential expression analysis for sequence count data [J].
Anders, Simon ;
Huber, Wolfgang .
GENOME BIOLOGY, 2010, 11 (10)
[3]
Comprehensive modeling of microRNA targets predicts functional non-conserved and non-canonical sites [J].
Betel, Doron ;
Koppal, Anjali ;
Agius, Phaedra ;
Sander, Chris ;
Leslie, Christina .
GENOME BIOLOGY, 2010, 11 (08)
[4]
miRGator v3.0: a microRNA portal for deep sequencing, expression profiling and mRNA targeting [J].
Cho, Sooyoung ;
Jang, Insu ;
Jun, Yukyung ;
Yoon, Suhyeon ;
Ko, Minjeong ;
Kwon, Yeajee ;
Choi, Ikjung ;
Chang, Hyeshik ;
Ryu, Daeun ;
Lee, Byungwook ;
Kim, V. Narry ;
Kim, Wankyu ;
Lee, Sanghyuk .
NUCLEIC ACIDS RESEARCH, 2013, 41 (D1) :D252-D257
[5]
miRDeep2 accurately identifies known and hundreds of novel microRNA genes in seven animal clades [J].
Friedlaender, Marc R. ;
Mackowiak, Sebastian D. ;
Li, Na ;
Chen, Wei ;
Rajewsky, Nikolaus .
NUCLEIC ACIDS RESEARCH, 2012, 40 (01) :37-52
[6]
Goff L., 2012, COMMERBUND ANAL EXPL
[7]
DAVID Bioinformatics Resources: expanded annotation database and novel algorithms to better extract biology from large gene lists [J].
Huang, Da Wei ;
Sherman, Brad T. ;
Tan, Qina ;
Kir, Joseph ;
Liu, David ;
Bryant, David ;
Guo, Yongjian ;
Stephens, Robert ;
Baseler, Michael W. ;
Lane, H. Clifford ;
Lempicki, Richard A. .
NUCLEIC ACIDS RESEARCH, 2007, 35 :W169-W175
[8]
The role of site accessibility in microRNA target recognition [J].
Kertesz, Michael ;
Iovino, Nicola ;
Unnerstall, Ulrich ;
Gaul, Ulrike ;
Segal, Eran .
NATURE GENETICS, 2007, 39 (10) :1278-1284
[9]
miRBase: integrating microRNA annotation and deep-sequencing data [J].
Kozomara, Ana ;
Griffiths-Jones, Sam .
NUCLEIC ACIDS RESEARCH, 2011, 39 :D152-D157
[10]
Conserved seed pairing, often flanked by adenosines, indicates that thousands of human genes are microRNA targets [J].
Lewis, BP ;
Burge, CB ;
Bartel, DP .
CELL, 2005, 120 (01) :15-20