-
With the release of EFO 3.23.0, there will be new phenotype data that we can integrate into the Platform to enrich the disease index and display on the disease profile page
-
**Preferred term label:**
Impaired ability to shift
**Synonyms**
Sticky behavior
Inflexible behavior - broad
Impaired set shifting
**Definition (free text, please give PubMed ID)**
A behavi…
-
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, …
-
As one can see for the following Item, Senior Theses Items imported from submissions for certificate programs are members of multiple collections, one being the departmental collection, the other bein…
-
We have a request from the Monogenic Diabetes GCEP to change a current MonDO ID for the gene INS for autosomal recessive inheritance.
The UUID for the curation is: https://curation.clinicalgenome.…
-
Hi,
for Uniprot release 2021-01 we require the following MONDO terms for mapping:
Not sure how the omim ingests work now on your end, so thought I'd raise this request. I have attached the DI de…
-
Hi @Mahmoud-Elbattah ,
First of all Thank you very much for sharing your work.
May I ask you to kindly share the `ASD.npz` as well or the script you used to create it?
I'm trying to run your ipy…
-
Can you share the dataset or the data source about where and how you get those? I need to do a class project for this, many thanks!
-
Rationale: better inferences
What is included: i.e only genes known to be disease-causing, not candidate genes. Not biomarkers
Metrics: increase in number of assignments (annotations and genes)
S…
-
- [x] Rough draft slides
- [x] Peer review with Primary members
- [x] Improve slides
- [x] add ideas such as "not all disabilities are the same","not all students learn the same way", "base…