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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
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?
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
The text was updated successfully, but these errors were encountered:
For question 1. The groups are made based on the 'category' variable you can include in the pheno-list.json, see step 4 in the README file. They just need to be strings, the names don't need to be ICD codes. I find it easiest to get my pheno-list.json by making a .csv file first and then doing the conversion. They show how this is done as the 1st of the 'other' methods to create the pheno-list.json https://github.com/statgen/pheweb/blob/df1530809e0821b53dd5feb1e405277d1a74c9bc/etc/detailed-loading-instructions.md#making-pheno-listjson TOPMED decides that however they want, ask them directly I suppose.
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
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.)?
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
The text was updated successfully, but these errors were encountered: