DiseaseMeth

DiseaseMeth provides a comprehensive repository and analytical platform for exploration and analysis of DNA methylation alterations associated with human diseases to support identification of differentially methylated genes (DMGs) and disease biomarkers.


Key Features:

  • Comprehensive Data Repository: Houses over 14,000 entries from more than 175 high-throughput experiments and gene-centric methylation data for 162 human diseases derived from multiple technologies and platforms.
  • Search Capabilities: Enables querying by gene ID and disease name to identify differentially methylated genes (DMGs) and gene-disease relationships.
  • Integrated Data Analysis: Provides cross-data set integration of methylation data for diseased and normal samples to facilitate identification of DMGs.
  • Functional Enrichment Tools: Includes FunctionSearch for functional enrichment using localized Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) annotations.
  • Unified Analysis Pipeline: Implements a unified analysis pipeline (version 3.0) to identify DMGs from stored original data, reporting 22,718 DMGs across 99 diseases.
  • Analytical Modules: Offers Methylation Disease Correlation and Cancer Prognosis & Co-Methylation modules for disease correlation and cancer prognosis/co-methylation analyses.
  • Experimental Associations from Literature: Incorporates manually curated experimentally confirmed associations mined from 1,472 PubMed papers, adding 448 new disease–methylation pairs.

Scientific Applications:

  • Biomarker Discovery: Identification of candidate disease biomarkers through analysis of DMGs across multiple diseases and datasets.
  • Disease Mechanism Studies: Investigation of the role of DNA methylation in disease initiation and progression.
  • Prognosis and Translational Research: Support for cancer prognosis assessment and development of personalized medicine approaches based on methylation patterns.

Methodology:

Integrates data from various sources including methylation-specific PCR and genome-wide profiling technologies, employs statistical analysis methods, and applies a unified analysis pipeline to identify DMGs from original data.

Topics

Details

Cost:
Free of charge
Tool Type:
web application
Operating Systems:
Linux, Windows, Mac
Added:
3/30/2017
Last Updated:
5/15/2022

Operations

Publications

Lv J, Liu H, Su J, Wu X, Liu H, Li B, Xiao X, Wang F, Wu Q, Zhang Y. DiseaseMeth: a human disease methylation database. Nucleic Acids Research. 2011;40(D1):D1030-D1035. doi:10.1093/nar/gkr1169. PMID:22135302. PMCID:PMC3245164.

Xing J, Zhai R, Wang C, Liu H, Zeng J, Zhou D, Zhang M, Wang L, Wu Q, Gu Y, Zhang Y. DiseaseMeth version 3.0: a major expansion and update of the human disease methylation database. Nucleic Acids Research. 2021;50(D1):D1208-D1215. doi:10.1093/nar/gkab1088. PMID:34792145. PMCID:PMC8728278.

PMID: 34792145
PMCID: PMC8728278
Funding: - National Natural Science Foundation of China: 31771601, 61972116, 6210070817, U20A20376 - Applied Technology Research and Development Project of Heilongjiang: GA20C018 - Heilongjiang Postdoctoral Fund: LBH-Z20158

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