read.fsa: Get fluorescence data from fsa files
In AFLP: Analysis of AFLP data

Read fluorescence data from fsa files.

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  read.fsa(path = "./", files = NULL, dye, SizeStandard,
    Breaks = NULL, Range = range(SizeStandard),
    binwidth = 1, SNR = 20, verbose = TRUE)

`files`	A vector of filenames. Can be a relative or an absolute path.
`path`	The base path for the filenames. Defaults to the working directory.
`dye`	A vector with the names of the dyes used for the data.
`SizeStandard`	A numeric vector with basepairs of the size standard.
`Breaks`	A named list with the breaks used for binning the fluorescence. If missing the breaks are estimated by read.fsa.bins()
`Range`	A numeric vector of length 2 with the lower and upper limit of the desired markers (in number of base pairs).
`binwidth`	The desired width of the bins.
`SNR`	Maximum signal-to-noise ratio for peaks of the size standard. Used to ignore unwanted very strong peaks.
`verbose`	Print the name of each file when processing it. Useful for tracking progress.