FDS

FDS quantifies functional divergence between orthologous human and mouse genes with emphasis on microRNA regulation.


Key Features:

  • Comprehensive evaluation: Assesses functional divergence by analyzing microRNAs regulating paired orthologous genes between human and mouse.
  • Gene-specific FDS values: Calculates a gene-specific Functional Divergence Score that is associated with evolutionary characteristics and expression divergence.
  • Drug target differentiation: Distinguishes between targets of approved drugs and targets that failed in clinical trials based on orthologous gene analysis.
  • Detailed functional and phenotypic insight: Reports functional and phenotypic differences for each orthologous gene pair.
  • Extensibility: Framework is adaptable to analyze orthologous genes between human and other species.

Scientific Applications:

  • Translational research: Quantifies cross-species functional differences to inform selection and interpretation of animal models for human disease studies.
  • Drug development: Identifies orthologous gene divergence that may underlie differential drug target behavior between human and mouse.
  • Evolutionary and genomic studies: Enables investigation of how gene functions and regulatory relationships, including microRNA interactions, have diverged between species.

Methodology:

Integrates microRNA regulation and gene expression pattern data to compute a gene-specific divergence score (FDS) for orthologous human–mouse gene pairs, with the score reflecting functional and phenotypic differences and associations with evolutionary characteristics and expression divergence.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Mac, Linux, Windows
Added:
11/28/2021
Last Updated:
11/28/2021

Operations

Publications

Cui C, Zhou Y, Cui Q. Defining the functional divergence of orthologous genes between human and mouse in the context of miRNA regulation. Briefings in Bioinformatics. 2021;22(6). doi:10.1093/bib/bbab253. PMID:34226920.

PMID: 34226920
Funding: - National Key Research and Development Program: 2020YFC2004704 - PKU-Baidu Fund: 2019BD014 - National Natural Science Foundation of China: 62025102, 81921001, 81970440, 82025008 - Peking University Basic Research Program: BMU2020JC001