Epidemiological tables
Want to analyze data from a prospectiv321 laddence") study, cohort study, case–control study, or matched case–control study? Stata's tables for epidemiologists make it easy to summarize your data and compute statistics such as incidence-rate ratios, incidence-rate differences, risk ratios, risk differences, odds ratios, and attributable fractions. You can analyze stratified data too—compute Mantel–Haenszel combined estimates, perform tests of homogeneity, and standardize estimates. If you have an ordinal rather than binary exposure, you can perform a test for a trend.

Survival analysis
Analyze duration outcomes—outcomes measuring the time to an event such as failure or death—using Stata's specialized tools for survival analysis. Account for the complications inherent in survival data, such as sometimes not observing the event (right-, left-, and interval-censoring), individuals entering the study at differing times (delayed entry), and individuals who are not continuously observed throughout the study (gaps). You can estimate and plot the probability of survival over time. Or model survival as a function of covariates using Cox, Weibull, lognormal, and other regression models. Predict hazard ratios, mean survival time, and survival probabilities. Do you have groups of individuals in your study? Adjust for within-group correlation with a random-effects or shared-frailty model. If you have many potential covariates, use lasso cox and elasticnet cox for model selection and prediction.

Linear, binary, and count regressions
Fit classical ANOVA and linear regression models of the relationship between a continuous outcome, such as weight, and the determinants of weight, such as height, diet, and level of exercise. If your response is binary, ordinal, categorical, or count, don't worry. Stata has estimators for these types of outcomes too. Use logistic regression to adjust odds ratios for confounding variables. Estimate incidence rates using a Poisson model. Analyze matched case–control data with conditional logistic regression. A vast array of tools is available after fitting such models. Predict outcomes and their confidence intervals. Test equality of parameters. Compute linear and nonlinear combinations of parameters.

Survey methods
Whether your data require a simple weighted adjustment because of differential sampling rates or you have data from a complex multistage survey, Stata's survey features can provide you with correct standard errors and confidence intervals for your inferences. Simply specify the relevant characteristics of your sampling design, such as sampling weights (including weights at multiple stages), clustering (at one, two, or more stages), stratification, and poststratification. After that, most of Stata's estimation commands can adjust their estimates to correct for your sampling design.

Marginal means, contrasts, and interactions
Marginal means and contrasts let you analyze the relationships between your outcome variable and your predictors, even when your outcome is binary, count, ordinal, or categorical. For instance, after you fit a logistic regression of a disease on an exposure variable and other covariates, your marginal means may be population-averaged risks. Or you can set the covariates to interesting values to compute adjusted risks and then use contrasts to get adjusted risk differences. After fitting almost any model in Stata, you can analyze the effect of covariate interactions and easily create plots to visualize those interactions.

Power, precision, and sample size
Before you conduct your experiment, determine the sample size needed to detect meaningful effects without wasting resources. Do you intend to compute CIs for means or variances or perform tests for proportions or correlations? Do you plan to fit a Cox proportional hazards model or compare survivor functions using a log-rank test? Do you want to use a Cochran—Mantel—Haenszel test of association or a Cochran—Armitage trend test? Use Stata's power command to compute power and sample size, create customized tables, and automatically graph the relationships between power, sample size, and effect size for your planned study. Or use the ciwidth command to do the same but for CIs instead of hypothesis tests by computing the required sample size for the desired CI precision. Or use gsdesign to compute stopping boundaries and the required sample sizes for group sequential designs. Instead of commands, use the interactive Control Panel to perform your analysis.

Meta-analysis
Combine results of multiple studies to estimate an overall effect. Use forest plots to visualize results. Use subgroup analysis and meta-regression to explore study heterogeneity. Use funnel plots and formal tests to explore publication bias and small-study effects. Use trim-and-fill analysis to assess the impact of publication bias on results. Perform cumulative and leave-one-out meta-analysis. Perform univariate, multilevel, and multivariate meta-analysis. Use the meta suite, or let the Control Panel interface guide you through your entire meta-analysis.

Causal inference
Estimate experimental-style causal effects from observational data. With Stata's treatment-effects estimators, you can use a potential-outcomes (counterfactuals) framework to estimate, for instance, the effect of family structure on child development or the effect of unemployment on anxiety. Fit models for continuous, binary, count, fractional, and survival outcomes with binary or multivalued treatments using inverse-probability weighting (IPW), propensity-score matching, nearest-neighbor matching, regression adjustment, or doubly robust estimators. If the assignment to a treatment is not independent of the outcome, you can use an endogenous treatment-effects estimator. In the presence of group and time effects, you can use difference-in-differences (DID) and triple-differences (DDD) estimators. In the presence of high-dimensional covariates, you can use lasso. If causal effects are mediated through another variable, use causal mediation with mediate to disentangle direct and indirect effects.

Multiple imputation
Account for missing data in your sample using multiple imputation. Choose from univariate and multivariate methods to impute missing values in continuous, censored, truncated, binary, ordinal, categorical, and count variables. Then, in a single step, estimate parameters using the imputed datasets, and combine results. Fit a linear model, logit model, Poisson model, multilevel model, survival model, or one of the many other supported models. Use the mi command, or let the Control Panel interface guide you through your entire MI analysis.

Multilevel mixed-effects models
Whether the groupings in your data arise in a nested fashion (patients nested in clinics and clinics nested in regions) or in a nonnested fashion (regions crossed with occupations), you can fit a multilevel model to account for the lack of independence within these groups. Fit models for continuous, binary, count, ordinal, and survival outcomes. Estimate variances of random intercepts and random coefficients. Compute intraclass correlations. Predict random effects. Estimate relationships that are population averaged over the random effects.

Bayesian analysis
Fit Bayesian regression models using one of the Markov chain Monte Carlo (MCMC) methods. You can choose from various supported models or even program your own. Extensive tools are available to check convergence, including multiple chains. Compute posterior mean estimates and credible intervals for model parameters and functions of model parameters. You can perform both interval- and model-based hypothesis testing. Compare models using Bayes factors. Compute model fit using posterior predictive values and generate predictions. If you want to account for model uncertainty in your regression model, use Bayesian model averaging.

Additive models of relative risk
Determine how exposures interact to put subjects at a higher risk of experiencing an outcome of interest. For example, you might be investigating how exposure to cigarette smoke and asbestos interact to increase the risk of lung cancer. With Stata's reri command, you can measure two–way interactions in an additive model of relative risk, while accounting for other risk factors. Choose from various supported models, such as binomial generalized linear, Poisson, negative binomial, logistic, Cox, parametric survival, and interval–censored parametric and semiparametric survival models. Estimate the relative excess risk due to interaction (RERI), attributable proportion (AP), and synergy index (SI).

Automated reporting and customizable tables
Stata is designed for reproducible research, including the ability to create dynamic documents incorporating your analysis results. Create Word or PDF files, populate Excel worksheets with results and format them to your liking, and mix Markdown, HTML, Stata results, and Stata graphs, all from within Stata. Create tables that compare regression results or summary statistics, use default styles or apply your own, and export your tables to Word, PDF, HTML, LaTeX, Excel, or Markdown and include them in your reports.

Jupyter Notebook with Stata
Jupyter Notebook is widely used by researchers and scientists to share their ideas and results for collaboration and innovation. It is an easy-to-use web application that allows you to combine code, visualizations, mathematical formulas, narrative text, and other rich media in a single document (a "notebook") for interactive computing and developing. You can invoke Stata and Mata from Jupyter Notebook with the IPython (interactive Python) kernel. This means you can combine the capabilities of both Python and Stata in a single environment to make your work easily reproducible and shareable with others.