TY - JOUR
T1 - RED-ML
T2 - a novel, effective RNA editing detection method based on machine learning
AU - Xiong, Heng
AU - Liu, Dongbing
AU - Li, Qiye
AU - Lei, Mengyue
AU - Xu, Liqin
AU - Wu, Liang
AU - Wang, Zongji
AU - Ren, Shancheng
AU - Li, Wangsheng
AU - Xia, Min
AU - Lu, Lihua
AU - Lu, Haorong
AU - Hou, Yong
AU - Zhu, Shida
AU - Liu, Xin
AU - Sun, Yinghao
AU - Wang, Jian
AU - Yang, Huanming
AU - Wu, Kui
AU - Xu, Xun
AU - Lee, Leo J.
PY - 2017/5
Y1 - 2017/5
N2 - With the advancement of second generation sequencing techniques, our ability to detect and quantify RNA editing on a global scale has been vastly improved. As a result, RNA editing is now being studied under a growing number of biological conditions so that its biochemical mechanisms and functional roles can be further understood. However, a major barrier that prevents RNA editing from being a routine RNA-seq analysis, similar to gene expression and splicing analysis, for example, is the lack of user-friendly and effective computational tools. Based on years of experience of analyzing RNA editing using diverse RNA-seq datasets, we have developed a software tool, RED-ML: RNA Editing Detection based on Machine learning (pronounced as "red ML"). The input to RED-ML can be as simple as a single BAM file, while it can also take advantage of matched genomic variant information when available. The output not only contains detected RNA editing sites, but also a confidence score to facilitate downstream filtering. We have carefully designed validation experiments and performed extensive comparison and analysis to show the efficiency and effectiveness of RED-ML under different conditions, and it can accurately detect novel RNA editing sites without relying on curated RNA editing databases. We have also made this tool freely available via GitHub . We have developed a highly accurate, speedy and general-purpose tool for RNA editing detection using RNA-seq data. With the availability of RED-ML, it is now possible to conveniently make RNA editing a routine analysis of RNA-seq. We believe this can greatly benefit the RNA editing research community and has profound impact to accelerate our understanding of this intriguing posttranscriptional modification process.
AB - With the advancement of second generation sequencing techniques, our ability to detect and quantify RNA editing on a global scale has been vastly improved. As a result, RNA editing is now being studied under a growing number of biological conditions so that its biochemical mechanisms and functional roles can be further understood. However, a major barrier that prevents RNA editing from being a routine RNA-seq analysis, similar to gene expression and splicing analysis, for example, is the lack of user-friendly and effective computational tools. Based on years of experience of analyzing RNA editing using diverse RNA-seq datasets, we have developed a software tool, RED-ML: RNA Editing Detection based on Machine learning (pronounced as "red ML"). The input to RED-ML can be as simple as a single BAM file, while it can also take advantage of matched genomic variant information when available. The output not only contains detected RNA editing sites, but also a confidence score to facilitate downstream filtering. We have carefully designed validation experiments and performed extensive comparison and analysis to show the efficiency and effectiveness of RED-ML under different conditions, and it can accurately detect novel RNA editing sites without relying on curated RNA editing databases. We have also made this tool freely available via GitHub . We have developed a highly accurate, speedy and general-purpose tool for RNA editing detection using RNA-seq data. With the availability of RED-ML, it is now possible to conveniently make RNA editing a routine analysis of RNA-seq. We believe this can greatly benefit the RNA editing research community and has profound impact to accelerate our understanding of this intriguing posttranscriptional modification process.
KW - A-to-I editing
KW - machine learning
KW - posttranscriptional modification
KW - RNA editing
KW - RNA-seq
UR - http://www.scopus.com/inward/record.url?scp=85020242524&partnerID=8YFLogxK
U2 - 10.1093/gigascience/gix012
DO - 10.1093/gigascience/gix012
M3 - Comment/debate
C2 - 28328004
AN - SCOPUS:85020242524
SN - 2047-217X
VL - 6
SP - 1
EP - 8
JO - GigaScience
JF - GigaScience
IS - 5
M1 - gix012
ER -