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Non-referenced genome assembly from epigenomic short-read data.
Kaspi, Antony; Ziemann, Mark; Keating, Samuel T; Khurana, Ishant; Connor, Timothy; Spolding, Briana; Cooper, Adrian; Lazarus, Ross; Walder, Ken; Zimmet, Paul; El-Osta, Assam.
Affiliation
  • Kaspi A; a Epigenetics in Human Health and Disease Laboratory ; Baker IDI Heart and Diabetes Institute ; The Alfred Medical Research and Education Precinct ; Melbourne , Victoria , Australia ;
Epigenetics ; 9(10): 1329-38, 2014 Oct.
Article in En | MEDLINE | ID: mdl-25437048
ABSTRACT
Current computational methods used to analyze changes in DNA methylation and chromatin modification rely on sequenced genomes. Here we describe a pipeline for the detection of these changes from short-read sequence data that does not require a reference genome. Open source software packages were used for sequence assembly, alignment, and measurement of differential enrichment. The method was evaluated by comparing results with reference-based results showing a strong correlation between chromatin modification and gene expression. We then used our de novo sequence assembly to build the DNA methylation profile for the non-referenced Psammomys obesus genome. The pipeline described uses open source software for fast annotation and visualization of unreferenced genomic regions from short-read data.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Analysis, DNA / DNA Methylation / Epigenomics Limits: Animals / Humans / Male Language: En Journal: Epigenetics Journal subject: GENETICA Year: 2014 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Sequence Analysis, DNA / DNA Methylation / Epigenomics Limits: Animals / Humans / Male Language: En Journal: Epigenetics Journal subject: GENETICA Year: 2014 Document type: Article
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