The
Illumina Copy Number Input Engine
imports copy number data from files generated by Illumina
®
BeadStudio software into a SAS data set that can be used as input for the advanced JMP Genomics analytical processes.
The
Full Data Table
presents data in the
tall
format, having markers represented in rows and individual samples presented in columns. The
Final Report file
presents the data in a
stacked
format: each marker/individual pair is presented in a separate row. You can import various copy number metrics from both types of files, including
log R Ratio
and
B Allele Freq
. Additional information about the individual samples and marker annotation can be imported from the
sample
and
map
files.
The following example uses a proprietary data set provided by
Illumina
. These files, which include the
Full Data Table.txt
full data file, the
Illumina_CNV370_Samples_Confidential.txt
final report file, and the
Samples Table.txt
sample file, were saved to an
Illumina
folder saved in the JMP Genomics
Sample Data
folder. Please contact Illumina for more information about this data set.