% Generated by roxygen2: do not edit by hand
 % Please edit documentation in R/sample_data.R
 \docType{data}

 \name{nucleosome_htseq}
 \alias{nucleosome_htseq}

 \title{Example reads from high-troughtput sequencing nucleosome positioning
 experiment}

 \format{\code{GRanges} with the range of the reads and a data column with the

 strand information.}

 \source{
 Publication pending

 }
 \description{

 Few reads from paired-ended MNase-seq experiment in S.cerevisiae where
 mononucleosomes were sequenced

 }
 \details{

 This data is obtained from MNase digested nucleosomal DNA and sequenced with
 Illumina platform. Paired-ended reads where mapped to SacCer1 genome using
 Bowtie, and imported to R using the package \code{ShortRead} and paired ends
 where merged into a single range.

 Reads were sorted by chromosome and starting position and only a few reads
 from the starting positions of chromosome 1 are presented.

 }
 \keyword{datasets}