There are many useful visualizations, annotations, and biological interpretation tools that can operate on a gene list. In order for these features work with an imported list, an annotation file must be associated with the gene list. Additionally, many operations that work with a list of significant genes (like GO- or Pathway-Enrichment) require comparison against a background of “non-significant” genes. The quickest way to accomplish both is to use the background of “all genes” for that organism provided by an annotation source like RefSeq, Ensembl, etc. in .pannot (Partek annotation), .gff, .gtf, .bed, tab- or comma-delimited format. If the file is not already in a tab-separated or comma delimited format, you may import, modify, and save the file in the proper file format.
Select File from the main toolbar
Select Genomic Database under Import (Figure 1)
Select the annotation file; in this example, we select a .pannot file downloaded from Partek distributed library file repository – hg19_refseq_14_01_03_v2.pannot
Delete or rearrange the columns as necessary; we have placed the column with identifiers (should be unique ID) that correspond to our gene list first
Select File then Save As Text File... to save the annotation file; we have named it Annotation File (Figure 2)
Now we can add the annotation file to our imported gene list.
Right click 1 (gene_list.txt) in the spreadsheet tree
Select Properties from the pop-up menu
This brings up the Configure Genomic Properties dialog (Figure 3).
Select Browse under Annotation File
Choose the annotation file; we have chosen Annotation File.txt
If this is the first time you have used an annotation, the Configure Annotation dialog will launch. This is used to choose the columns with the chromosome number and position information for each feature. Our example annotation file has chromosome, start, and stop in separate columns.
Select the proper column configuration options (Figure 4)
Select Close to return to the Configure Genomic Properties dialog
Select Set Column: to open the Choose column with gene symbols or microRNA names dialog (Figure 5)
Select the appropriate column; here the default choice of 1. Symbol is appropriate
Select OK to return to the Configure Genomic Properties dialog
Select the appropriate species and genome build options; we have selected Homo sapiens and hg19 (Figure 6)
Select OK
The annotation file has been associated with the spreadsheet and additional tasks can now be performed on the data, e.g. since the annotation has genomic location, you can draw chromosome view on this data.
If an annotation file has been associated with a spreadsheet, annotations from the file can be added as columns in the spreadsheet when each identifier is on a row.
Right click on a column header
Select Insert Annotation
Select columns to add from Column Configuration; we have selected Chromosome, Start, and Stop (Figure 7)
Select OK
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Select () to close the annotation file
Select () to save the spreadsheet
