ReadSample: ReadSample
In mbertalan/iPsychCNV: iPsychCNV

ReadSample: Read data.

1 2	ReadSample(RawFile = "Test.txt", skip = 0, LCR = FALSE, PFB = NULL, chr = NA, SNPList = NULL)

`RawFile:`	The raw data files, default = Test.txt.
`Skip:`	Integer, the number of lines of the data file to skip before beginning to read data, default = 0.
`LCR:`	List low copy repeat regions, list of SNPs that should be removed, default = FALSE.
`PFB:`	Vector, population frequency 0 to 1 for each SNP in the array, default = NULL.
`Chr:`	Character, select a specific chromosome to be analyzed, default = NA.
`SNPList:`	Getting Chr. and Position from another source than the RawFile - input should be the full path of the SNPList with columns: Name, Chr, amd Position. Any positions from the RawFile will be erased. A PFB-column is also allowed but will be overwritten by the PFB-parameter or exchanged with 0.5