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R4VN 1.6 adds egenvar() for flexible row-wise and
group-wise variable generation, distdata() for
distribution/probability calculations, and distlearn() for
interactive distribution teaching. It also incorporates the CRAN
resubmission changes concerning package availability checks, examples,
and user-controlled random seeds.
R4VN provides short commands for health-data management, descriptive and inferential statistics, epidemiological analysis, regression, publication Tables, export, and graphs.
patient <- opendata("patient.dta")
usedf(patient)
genvar(age2 = age^2)
tab1(sex, smoking, by = c(province, agegroup))
sum1(age, bmi, by = c(sex, agegroup))
describe(age2)
View(patient)Because patient was activated with
usedf(patient), R4VN data-editing commands update the
visible object as well as the active data.
egenvar() complements genvar() with
row-wise and grouped calculations.
egenvar(min_score = rowmin(q1:q5),
max_score = rowmax(q1:q5),
mean_score = rowmean(q1:q5))
egenvar(mean_bmi = mean(bmi), z_bmi = z(bmi), by = sex)distdata() acts as a compact probability calculator. For
discrete distributions, a single x automatically returns
equality and both tail probabilities. distlearn() launches
the interactive R4VN Distribution Learning Studio.
distdata("binomial", n = 10, x = 3, p = .20)
distdata("normal", mean = 100, sd = 15, lower = 85, upper = 115)
# Interactive teaching app
distlearn("binomial")tb <- tab(
vars = vars(c.age, b2.sex, q.bmi),
by = hypertension,
test = TRUE,
or = TRUE,
event = "Yes",
show = FALSE
)
tabexport(tb, export = c("html", "docx", "xlsx"), file = "report")tabsurv() uses a context-sensitive reporting profile by
default. A grouped call produces descriptive outcomes, Kaplan-Meier
estimates, automatically selected time-point risks, overall incidence
rates, group comparisons, RMST, a publication-ready graph, and
export-ready tables. Adding vars also activates Cox models
and proportional-hazards diagnostics.
Interpretation and the detailed life table are intentionally off by
default. Enable them explicitly with interpretation = TRUE
and lifetable = TRUE. For cumulative incidence at selected
times, use the direct shorthand cuminc = c(6, 12, 24); this
is 1-KM for ordinary survival and the Aalen-Johansen CIF for competing
risks.
surv_result <- tabsurv(
followup, death,
by = treatment,
vars = vars(c.age, b2.sex, stage, treatment),
data = patient,
failure = 1
)
# Optional narrative interpretation and event-time Kaplan-Meier life table.
surv_detail <- tabsurv(
followup, death, by = treatment, data = patient, failure = 1,
interpretation = TRUE, lifetable = TRUE
)
surv_detail$lifetable
# Cumulative incidence at 6, 12, and 24 follow-up units.
surv_ci <- tabsurv(
followup, death, by = treatment, data = patient, failure = 1,
cuminc = c(6, 12, 24), report = "custom"
)
surv_ci$cuminc
# Export every non-empty table from the same command.
tabsurv(
followup, death, by = treatment, data = patient,
failure = 1, export = "docx", file = "survival-report.docx"
)
# Use the concise R4VN 1.5 defaults when an older workflow requires them.
tabsurv(followup, death, by = treatment, data = patient,
report = "custom")Run help(package = "R4VN") or
?R4VN_examples for the complete cookbook.
tabmeta() accepts either study-level estimates or raw
outcome summaries. For a binary outcome, the four 2-by-2 cells can be
supplied directly; OR is inferred when no effect selector is specified.
The default automatic profile adds the appropriate prediction, few-study
inference, publication-bias and sensitivity modules, figures, and
export-ready tables.
meta_result <- tabmeta(
data = trials, study = study,
a = event_treat, b = non_event_treat,
c = event_control, d = non_event_control,
subgroup = region,
moderator = vars(c.year, design)
)
meta_result$estimates$overall
meta_result$tables$Statistical_tests
meta_result$tests$overall
meta_result$tests$heterogeneity
meta_result$tables$Subgroup_test
meta_result$tables$Meta_regression
meta_result$tables$Publication_bias
meta_result$tables$Small_sample_inferenceThe HTML Viewer remains the complete report. With
plot=TRUE, the forest plot is also drawn in the R/RStudio
Plot pane by default; use
plot_display=c("forest", "funnel", "trimfill") or
plot_display="all" to populate Plot history. The forest
plot has separate headed Estimate (95% CI) and Weight columns, with
Weight on the far right, and uses round parentheses. For direct
a,b,c,d input, plot(m, show_abcd=TRUE)
displays the four cells. Labelled subgroup codes use their value labels,
and the Viewer adds one clearly titled forest plot per subgroup level.
The same overall and subgroup forest plots are added to R/RStudio Plot
history, where Previous/Next reviews them. Meta-regression output prints
Intercept in full and uses moderator labels when available.
Each subgroup result contains the pooled-effect test and the full
heterogeneity test, with confidence intervals for I-squared and
tau-squared when estimable. For publication, these results are
transposed so statistics are rows and the few subgroup levels are
columns; $subgroup_long retains tidy one-row-per-group
data. Effect and meta-regression estimates use two decimals by default;
change this consistently with digit=. Restricting
xlim clips outlying graphical intervals with arrows while
retaining exact numerical annotations. Prediction intervals remain in
the result but are not drawn by default. Figures expose journal controls
for fonts, colors, symbols, shading, axes, contours, labels, size, and
resolution, while engine_args provides direct advanced
metafor controls.
Set interpretation=TRUE for sectioned interpretation of
the pooled result, heterogeneity, prediction interval,
subgroup/moderator tests, small-study effects, few-study inference,
influence, leave-one-out, and cumulative evidence.
Use ?tabmeta for complete examples covering OR/RR/RD,
subgroup analyses, moderators, meta-regression, cumulative
meta-analysis, small-study effects, few-study inference, figures, and
direct report export.
R4VN 1.5 keeps the compact R4VN syntax while adding quick vector data
entry, label-aware hierarchical grouping, richer distribution
diagnostics, Bonferroni and other post-hoc/effect-size inference,
combined labelled graph panels with
xline/yline, and model postestimation.
# Quick data entry: no data.frame() is required first
genvar(weight = c(29, 26, 13, 23, 23, 25, 17, 22))
ghist(x = weight, normal = TRUE, xline = mean(weight, na.rm = TRUE))
# One convention for nested grouping: final variable is the inner group
ttest(weight, by = vars(province, sex), effect = TRUE)
normtest(vars = vars(weight, age), by = vars(province, sex))
# Postestimation uses the most recently fitted R4VN model
logistic(outcome, c.age, i.sex, data = d)
margins(at = at(age = seq(30, 60, 5)))
marginsplot()
predict(newvar = phat, type = "probability")
# Regression diagnostics are opt-in
m <- regress(score, c.age, c.bmi, data = d, diagnosis = TRUE)
predict(m, type = "standardized")
predict(m, type = "studentized")
predict(m, type = "leverage")
predict(m, type = "cooksd")
predict(m, type = "dfbetas", term = "age")These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.
Health stats visible at Monitor.