Published March 15, 2021
| Version v1
Dataset
Open
VPMBench - A test bench for variant prioritization methods - Case Study Dataset
Description
This dataset contains the first 500 benign and 500 pathogenic SNPs from ClinVar
(release date: 2021-02-13) for the GRCh37 reference genome.
Files
Files
(455.0 kB)
| Name | Size | Download all |
|---|---|---|
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md5:ce9cf13c72ba5969873bd7692d212078
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455.0 kB | Download |