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Dear @spond,
I have encountered another problem while running GARD. Here is the part of the error messge.
> - __Analysis Version__: 0.1
>
> type: nucleotide
> rv: GDD
> How many site rate …
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High level epic to track all requirements related CEC RAS. including GARD, Callout and PLD check
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Currently Aarskog syndrome (DOID:6683) is in as a child of 'syndromic X-linked intellectual disability' and has an X-linked inheritance relationship. This is incorrect as:
1. Most patients with Aarsk…
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I am unable to make armory work in gpu mode on a system with CUDA 10.0, Python 3.6, using the twosixarmory/pytorch:0.6.0 docker container. I get no error when running the ucf101_baseline_pretrained co…
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Dear developers,
I am running GARD on alignment files, and GARD terminates with error messages for some of the alignments.
Here is the some part of the error message. How would this be happen…
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It would be nice to provide the parameter `include_children` to the `/rest/trait/all` endpoint.
Right now what I do, as an alternative, is to get all EFO identifiers with `/rest/trait/all` first, …
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Hi,
I have been trying unsuccessfully to use GARD on v2.5.0 and have been getting errors.
When I run '--type Nucleotide' the analysis finishes. The JSON file gets printed out but the 'best-gard'…
ghost updated
4 years ago
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this groups a generic disease and a gene-specific subtype
```
id: MONDO:0009696
name: juvenile myoclonic epilepsy
def: "Juvenile myoclonic epilepsy is the most common hereditary idiopathic gener…
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We currently have an entry for Potter Syndrome, GARD includes 3 subtypes. Should these be added? What is the relationship to OMIM:263200?
https://rarediseases.info.nih.gov/diseases/4462/potter-sequ…
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I submitted my DNA sequence on the DataMonkey, ready to do the GARD calculation, but after about a minute running, prompted me:
We're sorry, there was an error processing your job. Please try again,…