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The LoF project team have now shared their complete dataset with us for downstream use. The plan would be to add these data to the variant page (annotation).
I open this ticket for our own records an…
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### Submitter Name
Arpad Danos
### Submitter Affiliation
Washington University
### Submitter Github Handle
arpaddanos
### Additional Submitter Details
Staff Scientist at Griffith Lab
### Proje…
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### Submitter Name
Susanna Kiwala
### Submitter Affiliation
Washington University in St. Louis
### Submitter Github Handle
susannasiebert
### Additional Submitter Details
CIViC de…
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**Is your feature request related to a problem? Please describe.**
This is the list of Categories on Dockstore, though manual curation is slow:
```
COVID-19
Genomics Toolsets
Alignment
Assembly
Asso…
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### Submitter Name
Grace Pendlebury
### Submitter Affiliation
Shariant / Australian Genomics
### Submitter Github Handle
_No response_
### Additional Submitter Details
Shariant is…
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V1 was released in https://github.com/ClinGen/gene-and-variant-curation-tools/issues/22 (#22)
This ticket is for further updates, e.g. currently the linkouts to Hypothes.is are not optimal as they do…
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**Background**:
OncoKB™(https://www.oncokb.org) is a precision oncology knowledge base developed at Memorial Sloan Kettering Cancer Center that contains biological and clinical information about gen…
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Following the application of this feature in the GCI..the CDOWG meeting on 7/15/2020 expressed interest in providing a version of this for the VCI.
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Sub-ticket for gnomAD v4 update #47
The goal of this ticket is to do the "like for like" update of the VCI population tab from gnomAD v2 to v4 data, along with deprecating a few sections of the po…
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As part of adding a Provisional Evidence subtile, we want to add a description to the [Allele Frequency Reference Sets Tile help section](https://brcaexchange.org/help#allele-frequency-reference-sets)…
e-t-k updated
2 months ago