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Nat Methods ; 13(4): 322-4, 2016 Apr.
Article in English | MEDLINE | ID: mdl-26855363

ABSTRACT

We describe epiGBS, a reduced representation bisulfite sequencing method for cost-effective exploration and comparative analysis of DNA methylation and genetic variation in hundreds of samples de novo. This method uses genotyping by sequencing of bisulfite-converted DNA followed by reliable de novo reference construction, mapping, variant calling, and distinction of single-nucleotide polymorphisms (SNPs) versus methylation variation (software is available at https://github.com/thomasvangurp/epiGBS). The output can be loaded directly into a genome browser for visualization and into RnBeads for analysis of differential methylation.


Subject(s)
DNA Methylation , Epigenesis, Genetic , Genome, Human , High-Throughput Nucleotide Sequencing/methods , Polymorphism, Single Nucleotide/genetics , Sequence Analysis, DNA/methods , Software , Humans , Sulfites/chemistry
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