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TarPmiR: a new approach for microRNA target site prediction
Abstract
Motivation: The identification of microRNA (miRNA) target sites is fundamentally important for studying gene regulation. There are dozens of computational methods available for miRNA target site prediction. Despite their existence, we still cannot reliably identify miRNA target sites, partially due to our limited understanding of the characteristics of miRNA target sites. The recently published CLASH (crosslinking ligation and sequencing of hybrids) data provide an unprecedented opportunity to study the characteristics of miRNA target sites and improve miRNA target site prediction methods. Results: Applying four different machine learning approaches to the CLASH data, we identified seven new features of miRNA target sites. Combining these new features with those commonly used by existing miRNA target prediction algorithms, we developed an approach called TarPmiR for miRNA target site prediction. Testing on two human and one mouse non-CLASH datasets, we showed that TarPmiR predicted more than 74.2% of true miRNA target sites in each dataset. Compared with three existing approaches, we demonstrated that TarPmiR is superior to these existing approaches in terms of better recall and better precision. Availability and Implementation: The TarPmiR software is freely available at http://hulab.ucf.edu/research/projects/miRNA/TarPmiR/. Contacts: haihu@cs.ucf.edu or xiaoman@mail.ucf.edu Supplementary information: Supplementary data are available at Bioinformatics online.
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“These molecular events have changed potential targeting features [4] and have led to different target genes between miRNAs with the same seed sequence.”
From Hsa-mir-548 family expression in human reproductive tissues (2021) · cites this paper as [4]
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“For instance, miRTarCLIP (Chou et al., 2013) identifies miRNA target sites from the data generated by high-throughput sequencing of RNA isolated by crosslinking immunoprecipitation (HITS-CLIP) experiments (Chi et al., 2009; Licatalosi et al., 2008) and photoactivatableribonucleoside-enhanced…”
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Cited by
Sorted by citations
Hsa-mir-548 family expression in human reproductive tissues
Rooda, I., Kaselt, B., Liivrand, M., Smolander, O.-P., Salumets, A., & Velthut-Meikas, A. (2021) · BMC Genomic Data · doi:10.1186/s12863-021-00997-w · Cited by 17
Restraint Stress in Mice Alters Set of 25 miRNAs Which Regulate Stress- and Depression-Related mRNAs
Solich, J., Kuśmider, M., Faron-Górecka, A., Pabian, P., & Dziedzicka-Wasylewska, M. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21249469 · Cited by 13
Metadata
- Authors
- Ding, J., Li, X., & Hu, H.
- Affiliations
- 1 Department of Electrical Engineering and Computer Science
- 2 Burnett School of Biomedical Science, College of Medicine, University of Central Florida, Orlando, FL 32816, USA
- Venue
- Bioinformatics
- Publisher
- Oxford University Press (OUP)
- Published
- 2016-05-20
- Volume
- 32
- Issue
- 18
- Pages
- 2768-2775
- ISSN
- 1367-4811
- 1367-4803
- PMC
- PMC5018371
- Cited by
- 171
- References
- 3
- Language
- en
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