NmSEER V2.0
NmSEER V2.0 predicts 2'-O-methylation (2'-O-me or Nm) sites within mRNAs and various non-coding RNAs to identify post-transcriptional modification locations for studies of RNA function.
Key Features:
- Target modifications: Predicts 2'-O-methylation (2'-O-me or Nm) sites in mRNAs and non-coding RNAs.
- Training data: Uses a refined dataset derived from Nm-seq high-resolution profiling that maps Nm sites with single-nucleotide precision and enhanced sensitivity.
- Encoding strategy: Combines one-hot encoding, position-specific dinucleotide sequence profiles, and K-nucleotide frequency encoding to represent sequence features.
- Algorithm: Employs a random forest classifier identified as the most robust method.
- Model evaluation: Assessed by rigorous 5-fold cross-validation and independent evaluations.
- Performance metric: Reports an Area Under the Receiver Operating Characteristic curve (AUROC) of 0.862.
Scientific Applications:
- Identification of candidate Nm sites: Predicts potential 2'-O-methylation locations for downstream experimental or computational analysis.
- RNA biology studies: Supports exploration of the functional implications of 2'-O-methylation in RNA molecules.
- Gene expression regulation research: Facilitates investigation of relationships between Nm modifications and regulation of gene expression and other cellular processes.
Methodology:
Modeling used Nm-seq–derived datasets with feature encodings (one-hot, position-specific dinucleotide sequence profiles, K-nucleotide frequency); a random forest classifier was selected and evaluated by 5-fold cross-validation and independent testing, yielding AUROC=0.862.
Topics
Details
- Tool Type:
- command-line tool
- Added:
- 1/14/2020
- Last Updated:
- 1/4/2021
Operations
Publications
Zhou Y, Cui Q, Zhou Y. NmSEER V2.0: a prediction tool for 2′-O-methylation sites based on random forest and multi-encoding combination. BMC Bioinformatics. 2019;20(S25). doi:10.1186/s12859-019-3265-8. PMID:31874624. PMCID:PMC6929462.