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Copy file name to clipboardExpand all lines: docs/source/glossary.rst
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Endogenous Variable
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An endogenous variable is a variable in a regression equation such that the variable is correlated with the error term of the equation i.e. correlated with the outcome variable (in the system). This is a problem for OLS regression estimation techniques because endogeniety violates the assumptions of the Gauss Markov theorem.
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Local Average Treatment effect
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LATE
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Also known asthe complier average causal effect (CACE), is the effect of a treatment for subjects who comply with the experimental treatment assigned to their sample group. It is the quantity we're estimating in IV designs.
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Non-equivalent group designs
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NEGD
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A quasi-experimental design where units are assigned to conditions non-randomly, and not according to a running variable (see Regression discontinuity design). This can be problematic when assigning causal influence of the treatment - differences in outcomes between groups could be due to the treatment or due to differences in the group attributes themselves.
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Pretest-posttest design
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A quasi-experimental design where the treatment effect is estimated by comparing an outcome measure before and after treatment.
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Propensity scores
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An estimate of the probability of adopting a treatment status. Used in re-weighting schemes to balance observational data.
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Quasi-experiment
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An empirical comparison used to estimate the effects of a treatment where units are not assigned to conditions at random.
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2SLS
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An estimation technique for estimating the parameters of an IV regression. It takes its name from the fact that it uses two OLS regressions - a first and second stage.
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Propensity scores
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An estimate of the probability of adopting a treatment status. Used in re-weighting schemes to balance observational data.
Copy file name to clipboardExpand all lines: docs/source/quasi_dags.ipynb
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"cell_type": "markdown",
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"metadata": {},
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"source": [
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"One nice feature of this set up is that we can evaluate the claim of __strong ignorability__ because it implies that $T\\perp\\!\\!\\!\\perp X | PS(X)$ and this ensures the covariate profiles are balanced across the treatment branches conditional on the propensity score. This is a testable implication of the postulated design! Balance plots and measures are ways in which to evaluate if the offset achieved by your propensity score has worked. It is crucial that PS serve as a balancing score, if the measure cannot serve as a balancing score the collision effect can add to the confounding bias rather than remove it. "
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"One nice feature of this set up is that we can evaluate the claim of __strong ignorability__ because it implies that $Z\\perp\\!\\!\\!\\perp X | PS(X)$ and this ensures the covariate profiles are balanced across the treatment branches conditional on the propensity score. This is a testable implication of the postulated design! Balance plots and measures are ways in which to evaluate if the offset achieved by your propensity score has worked. It is crucial that PS serve as a balancing score, if the measure cannot serve as a balancing score the collision effect can add to the confounding bias rather than remove it. "
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