Open gedankenstuecke opened 8 years ago
Hmm we could have a worker that parses the SNP's paper abstracts/names, extracts all words that appear in the phenotype descriptions or names, and then creates a SnpPhenotypeLink (or sth. like that), to be displayed in another tab on the SNP's show-page
We could even then link the recommendify results - since the phenotypes are linked by similarity in recommendify we can start from the SnpPhenotypeLink and add other phenotypes
How close would this be towards "providing medical information" as a service, i.e., "dangerous territory"?
Yes, I think that sounds like a good idea. I don't think that those recommendations for phenotypes etc. would be medical information. It's not that we're generating any reports. So what about the below?
@gedankenstuecke You can assign this issue to me. ;)
Happy to do so! 👍
So far the phenotypes and the SNPs are rather independent from each other, making it hard to link one to the other. But in principle we already have the information needed to link them, at least in a really low level way: The papers attached to the SNPs might have the phenotype names in the title.
Using those we could link certain SNPs to phenotypes and vice versa link phenotypes to SNPs. I think that could make it more useful for people who are more into using openSNP for browsing their own genomes. What do you think?