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-1. Name of the power point report script:                                                 	
-PRONTO (rePort geneRator fOr iNpred Tumor bOards)
-2. All Clinical and meta data is stored in the file “InPreD_PRONTO_metadata.txt”. And the script will generate report for the samples with the column "Create_report==Y".
-3. The filtered variants are read from the TSOPPI file “..._small_variant_table_forQC.tsv” (should be generated within TSOPPI in the next version, until then we rename the file manually). 
-If this file does not exist in the TSOPPI results folder, the script will read from the file "..._small_variant_table.tsv" instead.
-4. The output results will be saved into a folder named with runID and the subfolder named with the DNA sample ID.                
-5. In the header to the right in PP report, it is printed “Clinical_diagnosis” (from the meta data file). If unavailable, the PCGR tumor type is printed on slide 4-7. 
-6. No “tumor type” is printed in the left grey box.
-7. In the upper grey box on the left in PP report, print from the meta data file: “sex”, age (calculated from “Year_of_birth”), “Year_of_diagnosis” and “Requisition_hospital”. 
-8. Year in upper left is the same as the sequencing year (printed from the sequenced run id).
-9. The script checks if there is a matching RNA in the “sample-list” file in TSOPPI. 
-Within the meta data file, it then looks for both DNA and RNA information in the column “Sample_material_id_PS”, and print on two lines as follows: DNA: “Sample_material_id_PS”, RNA: “Sample_material_id_PS”.
-10. The printed text in the header is in white color. Blue header is behind the orange header. Darker color of the orange header. 
-11. Smaller text (size 9) for the Bio material; ex “primary tumor, post-treatment”.
-12. Bigger text (size X) for RNA fusion and splice findings. 
-13. The script Does not print “N=xx» in the header in the table to the right. 
-14. Updated description on the first page: “Variants of uncertain significance (VUS) refer to variants with unknown/unclear/inconclusive/contradictory functional consequence in cancer. Level of evidence for experimental treatment follows ESCAT guidelines and will be defined by the respective study/trial.”. 
-Unclear is updated to uncertain in the sentence “Variant of uncertain significance (VUS)”.
-15. Updated description of CN: “CN=copy number (assumes ploidy 2).” in slide 5 to 7.
-16. Updates in the table slide 8: one column added with information from “change_summary”, and one column added with the MTB format.
-17. New template with ctDNA info in the last slide.
-18. Added "inpred_node=" in configure file, so that script will print the node name into the header of the Power point report automatically.
-19. Bigger text (size 7) for the fusion text and the MS status in slide 2,6,7.
-20. The text locations of the PP report on top right area are bit higher.
-21. Updated description on the slide 6-7 right lower area: "#Variant of uncertain significance (VUS)".