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### Description of feature
We need the SV querying module to annotate 👍 https://github.com/J35P312/SVDB#query
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Welcome to the Scout user meeting @9:00-10:30 am!
Location: On zoom: https://ki-se.zoom.us/j/61414401020?pwd=WitWeThraU16NzdXekRaRE1BWEhKUT09
Please help us fill the agenda with topics that may …
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egonw updated
4 years ago
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Add license information
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Hi, I am wondering about this argument to graphtyper genotype:
```
--avg_cov_by_readlen=value
File with average boverage by read length.
```
and several others. Can I leave that empty?
…
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https://seqr.broadinstitute.org/project/R0384_rare_genomes_project_gen/saved_variants/variant/SV0055753_x111681268_r0384_rar
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- [x] http simple auth in nginx.conf
- [x] add button (in settings, danger zone)
- [x] setup server in pipeline container
- [x] set up endpoint `/data/sync`
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Can we have the reads for the probing please
https://seqr.broadinstitute.org/project/R0380_cmg_gazda_wgs/saved_variants/family/F018919_gaz_447
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For the EJP-RD project we need (soon) a seperate portal for rare disease pathways which is at the moment a sub-part of the disease portal.
The Rare disease portal should get the logos from EJP-RD, El…
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The file we currently use for mapping Orphanet IDs to disease terms is from the Orphanet public download site but this only includes the rare diseases and not the common diseases that are also display…