Literature DB >> 22027613

Next generation sequencing in epigenetics: insights and challenges.

Emma Meaburn1, Reiner Schulz.   

Abstract

The epigenetics community was an early adopter of next generation sequencing (NGS). NGS-based studies have provided detailed and comprehensive views of epigenetic modifications for the genomes of many species and cell types. Recently, DNA methylation has attracted much attention due to the discovery of 5-hydroxymethyl-cytosine and its role in epigenetic reprogramming and pluripotency. This renewed interest has been concomitant with methodological progress enabling, for example, high coverage and single base resolution profiling of the mammalian methylome in small numbers of cells. We summarise this progress and highlight resulting key findings about the complexity of eukaryotic DNA methylation, its role in metazoan genome evolution, epigenetic reprogramming, and its close ties with histone modifications in the context of transcription. Finally, we discuss how fundamental insights gained by NGS, particularly the discovery of widespread allele-specific epigenetic variation in the human genome, have the potential to significantly contribute to the understanding of human common complex diseases.
Copyright © 2011 Elsevier Ltd. All rights reserved.

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Year:  2011        PMID: 22027613     DOI: 10.1016/j.semcdb.2011.10.010

Source DB:  PubMed          Journal:  Semin Cell Dev Biol        ISSN: 1084-9521            Impact factor:   7.727


  22 in total

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Review 4.  The role of replicates for error mitigation in next-generation sequencing.

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Review 5.  Combining topographical and genetic cues to promote neuronal fate specification in stem cells.

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Review 6.  The fate is not always written in the genes: epigenomics in epidemiologic studies.

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Review 7.  Toxicogenomics and cancer susceptibility: advances with next-generation sequencing.

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8.  Quantitative gene analysis of methylation and expression (Q-GAME) in fresh or fixed cells and tissues.

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9.  Genome-wide methylation analysis in Silver-Russell syndrome patients.

Authors:  A R Prickett; M Ishida; S Böhm; J M Frost; W Puszyk; S Abu-Amero; P Stanier; R Schulz; G E Moore; R J Oakey
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10.  Next generation sequence analysis and computational genomics using graphical pipeline workflows.

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Journal:  Genes (Basel)       Date:  2012-08-30       Impact factor: 4.096

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