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.