Import Genotype Data
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This user guide describes how to export copy number and genotype data using Partek's Report Plug-in for Illumina GenomeStudio Genotype Module for use in Partek Genome Suite. The GenomeStudio plug-in lets you export data into a project that can be opened in Partek Genome Suite open directly. It is the fastest and most consistent way to get fully annotated Illumina gene expression data into Partek.
Download the plug-in zip file
unzip the file, there is a folder called PartekReport which contains two .dll files --Partek.Common.dll and Partek.GeneExpression.GenomeStudio.dll, move the PartekReport folder to
C:\Program Files \Illumina\GenomeStudio 2.0\Modules\BSGT\ReportPlugins, if there is no ReportPlugins folder in BSGT folder, create one, the path and folder names have to be exactly match one described above (Figure 1).
In GenomeStudio genotype project:
Choose Analysis > Reports>Report Wizard from the main menu
Select Custom Report and choose Partek Report Plug-in from the drop-down list
Specify AnnotationName, do NOT include <> in the name, you can the same name as the .bgx file you imported the ddata with, or a unique name to your dataset
Figure 1. Configuring the GenomeStudio copy number report dialog
Leave all the others as default value (Figure 2) click Next
Specify the report file name, we recoommend to put the exported files in their own folder, which allows you to move thefolder instead of all the files individually.
Click Finish (Figure 2)
Figure 2. Specify output folder and file name
The output generate 9 files in the folder including a project file (.ppj), annotation file, summary file and 3 sets of Partek spreadshet file-- each spreadsheet consists of 2 files.
To open the report, launch Partek Genomics Suite, choose File > Open Project, browse to the .ppj file to open. There will be three spreadsheets opened (Figure 3)
Figure 3. Open project in Partek Genomics Suite
Spreadsheet 1 contains genotype calls, spreadsheet 2 contains log R ratio which is copy number in log scale, spreadsheet 3 contains B allele frequency.
To do copy number analysis, select spreadsheet 2 log R ratio, choose Copy number workflow, start from QA/QC section. Genotype spreadsheet will be used for Association and LOH workflow.
If you need additional assistance, please visit our support page to submit a help ticket or find phone numbers for regional support.
