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Code required to re-create analysis performed in Cheng et al., genomic imputation paired with SR/MA of COVID-19 outcome difference between cancer and non-cancer patients

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TKMarkCheng/scerc2

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SCERC2 data analysis

Code required to reproduce [Cheng and Morris et al.,eClinicalMedicine 2025].

folder structure

  • DEQA_templates = downloaded version of the data extraction and quality assessment table that our team members see on Covidence.
  • Code = any code, including bash, python, R scripts and notebooks.
  • data = The downloaded .csvs from Covidence
    • data extraction table when downloaded requires a suffix change to DE.csv to ensure uniqueness to find
    • please AVOID changing the files manually, and only read into and write from scripts to maximise reproducibility. When reading in to R, be reminded to set read.csv(check.names = FALSE) to avoid characters being altered.
    • /lineage is data used for lineage imputation.
  • output
    • contains figures, intermediate and final tables.
    • Tables that are intrinsic to the Data Extraction template are in /output/processed_tables, they include:
      • Baseline characteristics (Age and sex distribution of the cancer and non-cancer cohort respectively)
      • Co-morbidities
      • outcome tables which includes
        • Primary Cancer Site
        • Metastasis status
        • Treatment type
        • COVID variants
        • COVID vaccination status
    • the exception being /data/review_241469_20240110223959_DE_knownDx_peerReviewed.csv which is generated by data/0.1_Cleaning.Rmd as it is just a cleaning script.
  • team_members_automated.xlsx

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Code required to re-create analysis performed in Cheng et al., genomic imputation paired with SR/MA of COVID-19 outcome difference between cancer and non-cancer patients

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