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Hi!
I usually run rvtests for rare variant testing with no problems at all. However, only for some genes, I've been getting the following error message:
```
[INFO] Analysis begins with [ 15301 ]…
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The use case described in #57 will be used to identify requirements on the interfaces between the VP[^1] and the connected resources, on the data objects that are communicated, and the services that p…
mroos updated
3 months ago
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Hi Joelle,
I was testing out some of the new interaction analyses and found something that I can't really explain:
I'm looking at a quantitative imaging phenotype in UKB Europeans (N=33,000) and…
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We noticed that some references didn't format well and that it always happened when there was a consortium in the author list. Also, the consortium name was missing.
There is always the solution o…
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Hello,
Kindly requesting for your help,
I am trying to do an association analysis, both for rare and common variants, however as I try to do some variant level summaries using the code below, it run…
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When searching for specific variants, if the variant is not present in ExAC the use would get a page that stated it was not present and also provided the coverage for that region. This was helpful be…
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In `paramlink2`, we need to set the dfreq for diseaseModel.
For example:
`dm = diseaseModel(chrom = "AD", penetrances = c(0,1,1), dfreq = 1e-5)`.
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I can't find an issue for this, though it came up in the [Mischievous Nominals paper](https://aclanthology.org/2021.udw-1.14) - example (5):
- **We** pilots deserve a pay raise
- **You** guys dese…
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Hi developers,
While performing GWAS using fastGWA within GCTA on our pgen genetic data, some snps are removed (1960 out of 16084709, with sample size=9217). While forcing GCTA not to filter them u…
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Dear raremetal developers,
I really appreciate the work you are doing to develop and maintain raremetal. I am reaching out because I need some help to understand raremetal behaviour.
Recently, I…