4.8 Article

Differential DNA Methylation Analysis without a Reference Genome

期刊

CELL REPORTS
卷 13, 期 11, 页码 2621-2633

出版社

CELL PRESS
DOI: 10.1016/j.celrep.2015.11.024

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资金

  1. European Union [282510]
  2. ERA-NET project EpiMark (FWF) [I 1575-B19]
  3. ERA-NET project CINOCA (FWF) [I 1626-B22]
  4. Marie Curie Career Integration Grant (European Union's Seventh Framework Programme) [PCIG12-GA-2012-333595]
  5. DOC Fellowship of the Austrian Academy of Sciences
  6. Human Frontier Science Program long-term fellowship [LT000211/2014]
  7. Austrian Academy of Sciences

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Genome-wide DNA methylation mapping uncovers epigenetic changes associated with animal development, environmental adaptation, and species evolution. To address the lack of high-throughput methods for DNA methylation analysis in non-model organisms, we developed an integrated approach for studying DNA methylation differences independent of a reference genome. Experimentally, our method relies on an optimized 96-well protocol for reduced representation bisulfite sequencing (RRBS), which we have validated in nine species (human, mouse, rat, cow, dog, chicken, carp, sea bass, and zebrafish). Bioinformatically, we developed the Ref-FreeDMA software to deduce ad hoc genomes directly from RRBS reads and to pinpoint differentially methylated regions between samples or groups of individuals (http://RefFreeDMA.computational-epigenetics.org). The identified regions are interpreted using motif enrichment analysis and/or cross-mapping to annotated genomes. We validated our method by reference-free analysis of cell-type-specific DNA methylation in the blood of human, cow, and carp. In summary, we present a cost-effective method for epigenome analysis in ecology and evolution, which enables epigenome-wide association studies in natural populations and species without a reference genome.

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