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R/single.count.R
In NADfinder: Call wide peaks for sequencing data
#' Counts data for chromosome 18 for an experiment of a single pair of samples
#'
#' @name single.count
#' @docType data
#' @keywords data
NULL
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NADfinder documentation built on Nov. 8, 2020, 5:35 p.m.
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#' Counts data for chromosome 18 for an experiment of a single pair of samples
#'
#' @name single.count
#' @docType data
#' @keywords data
NULL
Try the NADfinder package in your browser
Any scripts or data that you put into this service are public.
R Package Documentation
Browse R Packages
We want your feedback!
Note that we can't provide technical support on individual packages. You should contact the package authors for that.
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