@Ghost, @axolotl and myself had a good talk this past weekend. We agreed to closely work together on a Genome-wide association study (GWAS) across all patient groups encompassing PFS, PSSD, PAS (Accutane) and possibly Lupron/GnRH analogs (if we can involve that group). We will be using high powered software and computing resources to perform what basically amounts to a scientific study, executed at the community level. We are hoping to find genetic variants which predict our condition, and possibly find similarities between our respective conditions at a genetic level. Of course, we hope that this information will help us and our scientists better understand what the genetic drivers may be that make us more susceptible to this/these syndrome(s) than others. If we do find something interesting, we will try to recruit a scientist to help us deepen our investigation and publish the results in a peer reviewed journal.
Now we need YOUR HELP: If you already have taken a 23andMe test, please download extract and rename your provided file so it is called
username_substance_23andme.txt
for example, mine would be called:
awor_finasteride_23andme.txt
This will help us track who is providing the data. Please then upload your raw data to the following link:
Please note that only you and us can see your uploaded data. You will also not be able to see the uploaded data of other users. If you do not already have 23andMe genomic data, please consider getting yours tested through the 23andMe service.
Thanks in advance for your support.