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Survival data will be additionally analyzed using Kaplan-Meier survival curves and the log-rank test.
Intervention period data will be additionally coded by whether the data is collected during an "active" intervention period or during an "inactive" intervention period (after completion of the FARGs).
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For studies that present RR by subgroups (for example, relative risk associated with Body Mass Index, kg/m ≥30) the data for each subgroup will be additionally extracted.
Survival data (e.g., institutionalization, mortality) will be additionally analyzed using Cox regression.
Additionally, data will be analyzed according to the per protocol principle.
Additionally, data will be modified to ensure that individual patients, hospitals or surgeons cannot be recognised and deposited in an open-access online data repository for others to analyse.
Additionally, these data will be available to explore important tissue-specific comparisons in gene expression patterns between the retina and the cornea, two clinically relevant ocular tissues.
Additionally, relevant data will be collected regarding any hospital admissions or interventions during the study period.
Additionally the data will be categorised according to a woman's cytology screening history prior to surgery (i.e. always normal, borderline, resolved abnormalities, CIN etc) and these different groups compared.
Additionally, quantitative data will be analyzed to get information about the acceptance of instruments and to get an impression about effect sizes and the differences between participating and refusing patients.
Additionally, no expression data will be reported for any genes which lack annotation within the current IWGSC release and any contig assemblies which are duplicated in the reference assembly will exhibit a reduced number of uniquely mapped reads.
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Justyna Jupowicz-Kozak
CEO of Professional Science Editing for Scientists @ prosciediting.com