PharmVar Survey - Aug 2020
What type of organization are you working with? (check all that apply)
How did you find out about PharmVar?
How often do you access PharmVar
Not at all
Does PharmVar provide information that is essential for your work?
I could get the information somewhere else
If you could get the information elsewhere, where would you get it?
Who have you recommended PharmVar to?
Which of these genes have you accessed?
Which genes should PharmVar add in the future?
Which of the following features/tools have you used?
Toggled between sequence start and ATG start count modes
Compare view (graphical CAVE tool)
Filter options (e.g. filter haplotypes for function, variants, etc...)
Which features should PharmVar add in the future?
Have you mentioned or cited PharmVar when you published?
Are you aware of the PharmVar GeneFocus reviews?
If you are aware of the GeneFocus reviews, how relevant are these to your work?
If you are aware of GeneFocus, which other genes should be covered?
Are you a PharmVar member?
Please tell us in 2-3 sentences of the importance of PharmVar to your work
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