Supplementary Data for DISCAN
<p>Supplementary data for "The frequency of somatic mutations in cancer predicts the phenotypic relevance of germline mutations". This entry includes two data tables, uploaded as compressed text files:</p> <ul> <li><strong>features.csv.gz</strong> contains all the covariates used to train the models. </li> <li><strong>phenotype_probabilities.csv.gz</strong> contains the Random Forest probabilities for 1,361 phenotypes</li> </ul> <p>Gene identifiers are reported as Entrez ID.</p>
ShareScore
40/100
Overall dataset sharing score
Score breakdown
These five areas show where the dataset supports — or may limit — practical reuse.
- Stewardship
- 4
- Harmonization
- 4
- Access
- 20
- Reuse readiness
- 8
- Engagement
- 4
Dataset details
- Repository
- zenodo
- Published
- September 14, 2022
- License
- cc-by-4.0
- DOI
- 10.5281/zenodo.7074775
Scored with release 0.9.0
ScienceDex for faculty
Your academic CV and NIH biosketch
Make your CV in your school's format and your NIH biosketch from it, then download both as Word files.