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Releases: BritRobin/ParseSNP

ParseSNP ver. 0.5 Beta

17 Mar 23:10

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This is a long overdue code re-evaluation, fixing issues around Visual Studios code optimises. I also found opening files with CoInitializeEx COINIT_APARTMENTTHREADED with COINIT_MULTITHREADED which fixed Dialog focus loss issues. I added the other two tables of the Type 2 Diabetes study I used as a demonstration of how the pathogenics function is supposed to work.

Type2Diabetes_Europe.PPI MD5 Hash: 31D571C6C3DF9260E04AC81916BBB5F8
Type2Diabetes_EastAsian.PPI MD5 Hash: 13212F699CB93921EDCD017B48BDA272
Type2Diabetes_SouthAsian.PPI MD5 Hash: B9F38C3028D6754ED0495748DDBD6C34

ParseSNP ver. 0.46 Beta

26 Jan 02:10

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This is a minor fix. In the executable, it fixes the bug where Ctrl+V could paste non-numeric characters into the RSID search box. The code now strips the non-numeric characters and writes the corrected string back to the search box and searches.
The SNPedia button .bmp was missing from the source as it had been on my desktop and was now gone. I created a new .bmp from scratch put it in the source directory and amended the .RC path

ParseSNP ver. 0.45 Beta

24 Jan 04:33

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Fixed pathogenics list to unsorted,(so you can compare what you entered to the data your entering)
Added WM_MOVE: redraw!
Added SNPedia lookup button for found SNPs
Added double click on pathogenics load RSID into search
Added icon on all dialogs

Still included a file I made that shows possible risk factors for type 2 Diabetes in Europeans: Type2Diabetes_EUR.PPI
MD5: 31D571C6C3DF9260E04AC81916BBB5F8

will add the other tables as .PPI files hopefully, real-world stress allowing...

ParseSNP ver. 0.40 Beta

26 Dec 03:36

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Adds save/load draft to pathogenics creation
Adds delete from list to pathogenics creation
Cleaned up pathogenics creation dialog
Added .MD5 file creation to pathogenics creation .PPI save
Removed some redundant code

Still included a file I made that shows possible risk factors for type 2 Diabetes in Europeans: Type2Diabetes_EUR.PPI
MD5: 31D571C6C3DF9260E04AC81916BBB5F8

will add the other tables as .PPI files soon.

ParseSNP ver. 0.31 Beta

19 Dec 03:44

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Fixes Sex determination for ancestry files.
Adds MD5 Hash for PPI file to pathogenics results
Still included a file I made that shows possible risk factors for type 2 Diabetes in Europeans: Type2Diabetes_EUR.PPI
MD5: 31D571C6C3DF9260E04AC81916BBB5F8

ParseSNP ver. 0.3 Beta

11 Dec 04:43

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Added: Merge function, whereby you can load your latest RAW DNA file and add any RSIDs it is missing from older files by different companies.
Fixes omitted enable for pathogenics on project load!
Added Sex field for loaded file
fixes lots of typos and spelling mistakes and cleans up GUI
various code fixes:
Still included a file I made that shows possible risk factors for type 2 Diabetes in Europeans: Type2Diabetes_EUR.PPI
MD5: 31D571C6C3DF9260E04AC81916BBB5F8

ParseSNP ver. 0.25 Beta

16 Nov 03:32

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ParseSNP ver. 0.25 fixes the fact that the raw files populate both alleles of X for males!
New result message for 'no read' [0/0].
Clears results window on file open or project open.

ParseSNP ver. 0.2 Beta

09 Nov 20:45

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ParseSNP ver. 0.2 Beta

ParseSNP ver. 0.2 Beta adds the Pathogenics feature which allows the user to create a file from research data and then load and run the file against any loaded SNPs. The results shown can be used to indicate genetic risk factors. The results can be exported to a text file. I have included a file I made that shows possible risk factors for type 2 Diabetes in Europeans: Type2Diabetes_EUR.PPI MD5: 31D571C6C3DF9260E04AC81916BBB5F8

I have also cleaned up the GUI and added a program icon.

ParseSNP ver. 0.1 Beta

19 Sep 18:53
04ba331

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Pre-release

This program is a work in progress...
The Project was built in Visual Studio 2022, and because of the C++ 17 settings, you MUST load the Solution once you open the project ie: double-click the SLN file.
Creating a Project will prompt for a project name this must be alphanumeric only. It in turn will become a folder under
C:\Users<username>\Documents\ParseSNP\Projects
The current DNA file will be copied there and project entries saved.
To load a project go into that directory and load the ProjectManifest.ptxt
Once a project is created only the ProjectManifest.ptxt file will be updated when you save it.

To delete a project entry double-click it and you will be prompted to delete?

Have fun, remember it's Beta and I may not be online for a bit...

thx Robin

v0.4 alpha

12 Mar 03:16

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v0.4 alpha Pre-release
Pre-release

Ancestry RAW data search tool, exports rsIDs loaded to ancestoryDNA file format