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Description
Hello,
Please forgive these naive questions as I am new to PheWAS analysis.
For the UK Biobank dataset, I have run a PHESANT (https://github.com/MRCIEU/PHESANT) analysis for a subgroup of individuals known to be carriers of mutations associated with a given trait of interest. In other words, I've let PHESANT test association of the group of carriers to non-carriers for all available UKB phenotypes. I have an output file that lists association test results for each of these tests, with associated beta, pvalue.
My questions are
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how can I convert the individual phenotypes to groups under related phecodes, such as I see in your plots on PheWeb instances (e.g. you have phenotypes color-coded / categorized into "infectious diseases","neoplams","neurological","circulatory system", etc.)?
- Can this grouping be done for all phenotypes or only those with ICD codes?
- In the TOPMED PheWeb instance, it says, for example, there were 1419 "broad" phecodes - how do they establish this, and how can I group my output tests to these broad phecodes?
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Could you please point me to code (preferably R code within PheWeb) that allows color-coded plotting of a 'phewas' manhattan coded by the groups I mentioned above?
Thank you so much for fielding my fairly naive questions!
Vamsee