Cell-Free Epigenome Atlas (CFEA)
Cell-Free Epigenome Atlas (CFEA) catalogs and standardizes cell-free DNA (cfDNA) epigenomic profiles—including 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), and nucleosome positioning (NP)—across human diseases to support comparative analysis and biomarker development.
Key Features:
- Epigenetic modalities: Includes cfDNA profiles for 5-methylcytosine (5mC), 5-hydroxymethylcytosine (5hmC), and nucleosome positioning (NP).
- Dedicated database: Aggregates human cell-free epigenomes spanning 27 different human diseases.
- Comprehensive data collection: Integrates cfDNA-based epigenome-wide profiles relevant for noninvasive disease diagnosis and classification.
- Standardized quality control: Implements bioinformatic pipelines for quality control and standardized data processing of cfDNA epigenomic datasets.
- Curated biological and clinical information: Manually curates associated biological and clinical metadata to enable comparison across disease stages such as early and metastatic cancer.
Scientific Applications:
- Liquid biopsy biomarker development: Supports development of cfDNA-based epigenetic signatures for noninvasive biomarkers.
- Disease detection and classification: Enables analysis of epigenetic alterations in cfDNA for disease detection and tumor classification.
- Comparative epigenomics across disease stages: Facilitates comparison of cfDNA epigenomes across stages including early versus metastasis.
- Molecular mechanism and translational research: Provides standardized datasets to study epigenetic mechanisms in human diseases and inform personalized medicine research.
Methodology:
Bioinformatic pipelines for quality control and standardized data processing of cfDNA-based epigenome-wide profiles.
Topics
Details
- Added:
- 11/14/2019
- Last Updated:
- 12/10/2020
Operations
Publications
Yu F, Li K, Li S, Liu J, Zhang Y, Zhou M, Zhao H, Chen H, Wu N, Liu Z, Su J. CFEA: a cell-free epigenome atlas in human diseases. Nucleic Acids Research. 2019;48(D1):D40-D44. doi:10.1093/nar/gkz715. PMID:31428785. PMCID:PMC6943076.
DOI: 10.1093/NAR/GKZ715
PMID: 31428785
PMCID: PMC6943076
Funding: - National Natural Science Foundation of China: 61871294, 61873193, 81822030
- Science Foundation of Zhejiang Province: LR19C060001
- Beijing Natural Science Foundation: 7172175
- Special Foundation for Key Basic Research of Wenzhou Institute of Biomaterials and Engineering: WIBEZD2017009-05
- CAMS Innovation Fund for Medical Sciences: 2016-I2M-1-001, 2017-I2M-3-004