ENCODE DCC
ENCODE DCC curates and distributes genome-wide functional genomics datasets to catalog functional elements in the human and mouse genomes.
Key Features:
- Central repository: houses high-throughput, genome-wide datasets generated by ENCODE investigators, including ChIP-Seq, RNA-Seq, and DNA digestion assays.
- Sequencing data: provides raw sequencing reads with associated quality scores.
- Read alignments: supplies alignments of sequencing reads to reference genomes.
- Signal tracks: computes signals derived from read alignments.
- Element/peak calls: provides element or peak calls calculated from signal data.
- Uniform processing pipelines: implements uniform data processing pipelines for standardized analyses.
- Metadata capture: records detailed experimental parameters for each assay.
- Integration of assays: incorporates new data and assays into the repository.
- Cell-state indicators: includes datasets relevant to transcription factor-binding sites, histone modifications, chromatin accessibility, DNA methylation, RNA expression, and RNA binding.
Scientific Applications:
- Cataloging functional elements: enabling systematic identification and annotation of functional genomic elements in human and mouse genomes.
- Transcription factor mapping: supporting identification of transcription factor-binding sites from ChIP-Seq data.
- Histone modification profiling: enabling analysis of histone modification patterns across cell types.
- Chromatin and methylation assessment: supporting analyses of chromatin accessibility and DNA methylation states.
- Transcriptome and RNA binding analysis: enabling quantification of RNA expression and mapping of RNA-binding events from RNA-Seq and related assays.
- Standardized downstream analyses: providing consistently processed data for comparative, integrative, and computational method development.
Methodology:
Provision of sequencing reads with quality scores, read alignments, generation of signals from alignments, and element/peak calling performed via uniform data processing pipelines.
Topics
Details
- Tool Type:
- web application
- Added:
- 3/27/2017
- Last Updated:
- 12/25/2020
Operations
Publications
Raney BJ, Cline MS, Rosenbloom KR, Dreszer TR, Learned K, Barber GP, Meyer LR, Sloan CA, Malladi VS, Roskin KM, Suh BB, Hinrichs AS, Clawson H, Zweig AS, Kirkup V, Fujita PA, Rhead B, Smith KE, Pohl A, Kuhn RM, Karolchik D, Haussler D, Kent WJ. ENCODE whole-genome data in the UCSC genome browser (2011 update). Nucleic Acids Research. 2010;39(suppl_1):D871-D875. doi:10.1093/nar/gkq1017. PMID:21037257. PMCID:PMC3013645.
Rosenbloom KR, Dreszer TR, Pheasant M, Barber GP, Meyer LR, Pohl A, Raney BJ, Wang T, Hinrichs AS, Zweig AS, Fujita PA, Learned K, Rhead B, Smith KE, Kuhn RM, Karolchik D, Haussler D, Kent WJ. ENCODE whole-genome data in the UCSC Genome Browser. Nucleic Acids Research. 2009;38(Database):D620-D625. doi:10.1093/nar/gkp961. PMID:19920125. PMCID:PMC2808953.
Luo Y, Hitz BC, Gabdank I, Hilton JA, Kagda MS, Lam B, Myers Z, Sud P, Jou J, Lin K, Baymuradov UK, Graham K, Litton C, Miyasato SR, Strattan JS, Jolanki O, Lee J, Tanaka FY, Adenekan P, O’Neill E, Cherry JM. New developments on the Encyclopedia of DNA Elements (ENCODE) data portal. Nucleic Acids Research. 2019;48(D1):D882-D889. doi:10.1093/nar/gkz1062. PMID:31713622. PMCID:PMC7061942.