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Trying to mass query all phenotypes in the KG by setting query to NULL and raising limit.
Running with limit
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Hi everyone
This is more of a request for help/pointers than an issue.
Has anyone attempted dockerizing/implementing parallelisation for Regenie Phase I? I have found some tips in the wiki but n…
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### Discussed in https://github.com/Data4DM/BayesSD/discussions/192
Originally posted by **hyunjimoon** February 22, 2024
Q1. there's difference between voluntary environment change (update ph…
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@ValWood @kimrutherford
I was doing a CC today and the author has annotated double mutants cdc15+[wt level] pom1-as1[wt level] to capture the fact that in pom1-as1 you have abnormal protein localis…
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### Problem Statement
Multiple US electronic Clinical Quality Measure (eCQM) require datetime calculations when doing computations from electronic health records. Public domain examples are publish…
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Some data sources provide only very broad location information about a sequence alteration (i.e at the level of a chromosome region instead of within a specific gene/marker). @nlwashington can provid…
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### 2022-09-16 @rays22, @souzadevinicius, @ar-ibrahim, @matentzn
- [ ] Why is there no 'abnormal femur' class in uPheno? - These should be automatically generated?
- [ ] 'decreased length femur': …
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given a set of phenotype profiles, find the profile in common...the graph intersection. :)
i believe this would use the compare owlsim call, and it would give you back the set of phenotypes in commo…
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Related to duplicated gene-disease issue #735.
Recreate: From phenotype http://beta.monarchinitiative.org/phenotype/ZP:0007522, go to Genes tab. Count is 4, but all four are the same gene/associatio…
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