Code and summary results for: The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants

Name: Code and summary results for: The phers R package: using phenotype risk scores based on electronic health records to study Mendelian disease and rare genetic variants
Creator: figshare
Published: 2022-06-07 15:06:43
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DataCite Commons2022-06-07 更新2024-07-29 收录

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https://figshare.com/articles/dataset/Code_and_summary_results_for_The_phers_R_package_using_phenotype_risk_scores_based_on_electronic_health_records_to_study_Mendelian_disease_and_rare_genetic_variants/20016728

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Zip file contains code, parameters, and output, but not the individual-level data.

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figshare

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2022-06-07