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NCBI Epigenomics

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Title: NCBI Epigenomics  
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NCBI Epigenomics

NCBI Epigenomics
Content
Description epigenomic data sets.
Contact
Research center National Center for Biotechnology Information
Authors Ian M Fingerman
Primary citation Fingerman & al. (2011)[1]
Release date 2010
Access
Website http://www.ncbi.nlm.nih.gov/epigenomics
Tools
Miscellaneous
The Epigenomics database at the National Center for Biotechnology Information is a database for whole-genome epigenetics data sets.[1]

Contents

  • The Epigenomics Database 1
    • Content of Epigenomics database 1.1
    • Database Use 1.2
      • Experiment Search 1.2.1
      • Sample Search 1.2.2
      • Database Navigation and Usage Help Resources 1.2.3
  • Roadmap Epigenomics Project 2
  • The Epigenome 3
  • See also 4
  • References 5
  • External links 6

The Epigenomics Database

The Epigenomic Database of the National Center for Biotechnology Information (NCBI) at the National Institutes of Health (NIH) was launched in June 2010 as a means to collect maps of epigenetic modifications and their occurrence across the human genome.[2] This database provides a publicly available resource for maps in stem cells and primary ex vivo tissues that detail genome-wide landscapes of epigenetic factors that occur in human development and disease.[1]

Content of Epigenomics database

The primary resources for the content of the Epigenomics Database are derived from two archival databases at the NCBI: The Gene Expression Omnibus (GEO) and the Sequence Read Archive (SRA).[1] The Gene Expression Omnibus is a data system for high-throughput genomic data that is generated from microarray and next-generation sequencing technologies.[3] Data used in the Epigenomics database is a combination of GEO and SRA subsets that are specific to Epigenetic factors. This data is subjected to additional review and organized in a more easily attainable fashion before added to the Epigenomics database.[1]

Database Use

All of the experiments and corresponding samples in the Epigenomics database are displayed in the default browser. As of October 2013, there are currently 4112 experiments and 1257 samples available in the database.[4] Five studied species are represented in the database, and many data tracks are available including expression of micro and small RNAs, histone modification and histone modifying enzymes, chromatin accessibility and chromatin associated factors, and transcription factors.[1] One such example from the database is a study of certain epigenetic factors in Drosophila melanogaster at the 20-24 hour embryonic stage of development.[5]

The Epigenomics database browser contain two fundamental search records, "Experiments" and "Samples".

Experiment Search

The Experiment search record refers to one or more experiments with a set of scientific aims.[1] Here a user is able to retrieve full data source information. This information includes the institution of the submitter, links to the original data submissions in GEO and SRA, links to literature citations in PubMed and/or full text articles in Pubmed.[1] Experiment records contain a unique accession number that includes a prefix 'ESS'.[1]

Sample Search

The sample search record corresponds to the biological material examined in a given experiment in the database and provides details about source attributes with values from controlled vocabularies.[1] There are over 20 biological attribute fields available, and among these fields include strain, cultivar, ecotype, individual, gender, age, developmental stage, cell line, cell type, tissue type, and health status.[1]

Database Navigation and Usage Help Resources

There are many available resources online for help in navigating and using the Epigenomics database. The "Epigenetics Help" section of the NCBI help manual contains information on the searchable database and provides a user with tools to use, manage, download and upload, and navigate the database.[6] There are also guides to navigation of the database aimed at specific researchers and fields of study, such as stem cell research.[7]

Roadmap Epigenomics Project

In 2007 the National Institutes of Health (NIH) launched the Roadmap Epigenomics Project. The aim of the project is a development of publicly available reference epigenome maps from a variety of cell types.[1] These epigenetic maps are intended to provide resources for studies of epigenetic events that underline human development, diversity, and disease.[8] For similar efforts see the ENCODE(ENCyclopedia Of DNA Elements) Project, whose initiatives are complementary to the Roadmap Epigenomics Project.[9]

The Epigenome

The

  • http://www.ncbi.nlm.nih.gov/epigenomics
  • http://www.nihroadmap.nih.gov/epigenomics
  • http://www.ncbi.nlm.nih.gov/geo/

External links

  1. ^ a b c d e f g h i j k l Fingerman, Ian M; McDaniel Lee; Zhang Xuan; Ratzat Walter; Hassan Tarek; Jiang Zhifang; Cohen Robert F; Schuler Gregory D (Jan 2011). "NCBI Epigenomics: a new public resource for exploring epigenomic data sets". Nucleic Acids Res. (England) 39 (Database issue): D908–12.  
  2. ^ "Overview". National Institutes of Health. Office of Strategic Coordination- The Common Fund. Retrieved 22 September 2013. 
  3. ^ Sayers, EW; Et. al (January 2010). "Database resources of the National Center for Biotechnology Information.". Nucleic Acids Research 38: D5–D16.  
  4. ^ http://www.ncbi.nlm.nih.gov/epigenomics. Retrieved 20 October 2013. 
  5. ^ Negre, N; Morrison CA; Shah PK; Bild NA; White KP (12 May 2009). "Genome-wide maps of chromatin state in staged Drosophila embryos, ChIP-seq". modENCODE. GSE16013. Retrieved 17 November 2013. 
  6. ^ Bethesda (MD) (2010). Epigenomics Help. US National Library of Medicine: National Center for Biotechnology Information (US). 
  7. ^ Karnik, R; Meissner A. (3 July 2013). "Browsing (Epi)genomes: a guide to data resources and epigenome browsers for stem cell researchers.". Cell Stem Cell 1: 14–21.  
  8. ^ Bernstein, Bradley E; Bradley E Bernstein, John A Stamatoyannopoulos, Joseph F Costello, Bing Ren, Aleksandar Milosavljevic, Alexander Meissner, Manolis Kellis, Marco A Marra, Arthur L Beaudet, Joseph R Ecker, Peggy J Farnham, Martin Hirst, Eric S Lander, Tarjei S Mikkelsen & James A Thomson (13 October 2010). "The NIH Roadmap Epigenomics Mapping Consortium". Nature Biotechnology 28 (10): 1045–1048.  
  9. ^ "The ENCODE (ENCyclopedia Of DNA Elements) Project". Science 306 (5696): 636–40. 22 October 2004.  
  10. ^ Bernstein, Bradley E; Alexander Meissner and Eric S. Lander (19 December 2011). "The Mammalian Epigenome". Cell. 4 128: 669–681.  
  11. ^ Russo, Vincenzo EA, Robert A. Martienssen, and Arthur D. Riggs. (1996). Epigenetic Mechanisms of Gene Regulation. Cold Spring Harbor Laboratory Press. p. Abstract.  
  12. ^ Costa, Fabricio F. (29 February 2008`). "Non-coding RNAs, epigenetics and complexity". Gene 410 (1): 9–17.  

References

See also

[12].Non-coding RNA as well as involvement of [11] structure,chromatin, and Gene silencing, DNA methylation changes involve methods of altering gene expression that do not involve changes in the underlying primary DNA sequence; these include epigenetic These [10]

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