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https://bioentity.link//#/publication/10.1093/genetics/iyaa010
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Similar to the work on variant index (#3350), we would like to serve a `gwas_study_index` dataset through OS + API.
This dataset is created by different upstream ETL processes ([gentropy](https://g…
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MSID: 91988
Version: 2
Preprint DOI: https://doi.org/10.1101/2023.10.04.560841
## Step 1. Awaiting reviews
**Editorial to post reviews via hypothesis**
**Useful links:**
- DocMap: https://data-hu…
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## Done Condition (What do we need? Why do we need it? Keep this is small as possible!)
Add manual checks here (https://mskconfluence.mskcc.org/pages/viewpage.action?spaceKey=CDSI&title=Sophia+Genetic…
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No idea why, this could / should just take the project ID from searching for bams:
https://github.com/eastgenomics/Genetics_Ark/blob/502bc5c2b5d2934411b7b32fce5a3776f087c6d1/cron/find_dx_data.py#L3…
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The article you published, "Deep learning predicts DNA methylation regulatory variants in the human brain and elucidates the genetics of psychiatric disorders," has been very helpful to me. However, u…
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This issue is intended to initiate discussion on how Translator clinical KPs can best leverage the genetics knowledge available via the Translator Genetics Provider.
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Hey guys,
I am struggling to find some good illustrations to:
`short reads`
`long reads`
`CNV`
`STR`
`SV`
`SNPs`
`indels`
Thank you very much for your amazing work!!
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Two datasets (ALS and Parkinson's) are to be made available for download via NeuroHub (CBRAIN data access methods).
Dataset files have been copied from their source locations from the lab of G. Rou…
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Hi does this work with realistic horse genetics?