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Supplementary Data for DISCAN

<p>Supplementary data for &quot;The frequency of somatic mutations in cancer predicts the phenotypic relevance of germline mutations&quot;. 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.&nbsp;</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

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