valr provides tools to read and manipulate intervals and signals on a genome reference. valr was developed to facilitate interactive analysis of genome-scale data sets, leveraging the power of dplyr and piping.
To learn more about valr, start with the vignette:
browseVignettes(package = "valr")
Jay Hesselberth [email protected]
Kent Riemondy [email protected]
Report bugs at https://github.com/rnabioco/valr/issues
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