Imports array data to MAD
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file |
A pennCNV-style file |
NumCols |
The number of columns in 'file' |
GenoCol |
The column in 'file' containing genotypes |
log2ratioCol |
The column in 'file' containing log2ratio intensities |
name.geno |
the name of the genotypes (default "AA", "AB" and "BB) |
chrs |
The names of the chromosomes. Default 1, ..., 22, X, Y |
MarkerIdCol |
The column in 'file' containing the name of the marker. Default first column |
ChrNameCol |
The column in 'file' containing the chromosome. Default second column |
ChrPosCol |
The column in 'file' containing the genomic position. Default third column |
sort |
should data be sorted by genomic position? The default is TRUE. |
orderProbes |
used to avoid sorting |
sep |
how data columns are separated. Default by tab |
saveGenInfo |
Should annotation data be saved? The default is TRUE. See details |
BAFCol |
The column in 'file' containing B-allele frequency (BAF) |
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