SysID usage survey
This is a short survey to get a better understanding of the current SysID usage.
The ideas collected here will be used for upcoming changes and improvements to the database.
How do you use SysID?
To quickly find information on single NDD entities
To generate filter lists for diagnostic sequencing
To stay informed about new NDD genes and phenotypes
For own research (e.g. pathway analyses etc.)
How frequent do you use the website?
once a week
once a month
with every update
Which table do you most often use?
Human Gene Info
Primary ID genes
Candidate ID genes
Do you use the 9 "Main clinical classes"?
Do you use the gene search option in the navbar?
Please rate your overall website user experience:
How do you currently access the SysID data?
Download tables as CSV file via the export option
Data scraping the website (e.g. computer program extracts the data)
Do you have other feature requests and suggestions (e.g. API, possibility to request a gene,..)?
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