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Copy file name to clipboardExpand all lines: TODO.md
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|`ContinuousDiD` CGBS-2024 remaining extensions (earlier phases — `covariates=` reg/dr, `treatment_type="discrete"`, single-cohort `control_group="lowest_dose"` with estimand `ATT(d)−ATT(d_L)` — are already supported; see REGISTRY Note #7). Remaining (all deferred `NotImplementedError`, documented): `estimation_method="ipw"` on the dose curve (scalar-adjustment / degenerate); `covariates=` × `survey_design=` (weighted OR + weighted nuisance IF); multi-cohort **heterogeneous-support** discrete aggregation (support-aware: average each dose only over the cohorts that observe it); **multi-cohort `lowest_dose`** (within-cohort `d_L` reference + support-aware cross-cohort aggregation); and **`covariates=` × `lowest_dose`** (conditional-PT-relative-to-`d_L` estimand). Single-cohort / 2-period / shared-support multi-cohort are supported. |`continuous_did.py`| CGBS-2024 | Heavy | Low |
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| `WooldridgeDiD` does not apply the W2025 Sec 5.4 `D_{G_max} x X` covariate normalization, and three sibling covariate rank deficiencies are pre-existing. Measured with the period range pinned and only the never-treated units toggled: (1) time-invariant `exovar` is absorbed by the unit FE, 4 of 26 columns, IDENTICALLY with and without never-treated units; (2) `xgvar`'s cell x covariate block, 19 of 41, identical on both panels; (3) `xtvar` under `demean_covariates=False` does exhibit the `sum_g D_g x = x` dependency that the default demeaning removes; (4) the newly-reachable case -- time-VARYING data passed through `exovar`, which its own docstring reserves for time-invariant covariates -- where the paper's `dT_i` rule would give a deterministic `D_{G_max} x X` drop instead of QR's arbitrary pick (coefficients unaffected, `1.35e-14`; `rank_deficient_action="error"` raises). REGISTRY's narrowed Sec 5.4 note cross-references this row. **Trap for whoever takes it:** `xtvar` under the DEFAULT `demean_covariates=True` is FULL RANK -- the raw block carries demeaned values while `D_g x X` carries raw ones -- and forcing the drop there moves `overall_att` 1.11903 -> 1.46269. Pinned as-is by `TestComparisonSupportFiltering::test_cells_derived_groups_did_not_leak_into_the_design`. | `diff_diff/wooldridge.py` | #729-followup | Heavy | Medium |
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|`WooldridgeDiD.n_control_units` counts never-treated UNITS on `control_group="never_treated"` regardless of method, but on the nonlinear paths (`logit`/`poisson`) treated units' pre-treatment rows ARE the identifying comparison -- only the OLS path absorbs them into their own cells. So the reported count under-states the comparison pool exactly where the REGISTRY control-pool asymmetry note applies. Widen to `not_yet_treated or (never_treated and method != "ols")`, or document the count as never-treated-units-by-definition. Behavior is PRE-EXISTING; documented for now in the REGISTRY control-pool Note rather than changed, because widening moves a public results field and wants its own ledger row and test matrix. |`diff_diff/wooldridge.py`|#729-followup | Mid | Low |
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|`WooldridgeDiD` has no opt-out for comparison-support period filtering: a user who would rather see the refusal than a reduced sample cannot ask for it. Adding one means a constructor parameter (`get_params`/`set_params` propagation, transactional validation), a ledger row, and a test matrix across both predicate branches and all three `rank_deficient_action` modes -- deliberately out of scope for the change that introduced the filter. The always-on warning is the interim answer. |`diff_diff/wooldridge.py`|#729-followup | Mid | Low |
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| Bad-control imputation estimator (Caetano et al. 2026 Section 6.1, Eqs. 5-7, S8 influence function) on a CallawaySantAnna `estimation_method="reg"` host: two untreated-sample OLS fits per cell plus the generated-regressor IF line. |`staggered.py`| bad-controls PR-B | Heavy | Low |
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| Bad-control SC "parallel trends for X" variant (Caetano et al. 2026 Section 7 / S17): a linearity-based alternative to covariate unconfoundedness with its own estimand. |`dml_did.py`| bad-controls PR-B | Heavy | Low |
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|`ATT_X(g,t)` event-study aggregation + bootstrap replay for the bad-control pre-test (today analytical per-cell only; never aggregated). |`dml_did_results.py`| bad-controls PR-B | Mid | Low |
Copy file name to clipboardExpand all lines: diff_diff/guides/llms.txt
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- [EfficientDiD](https://diff-diff.readthedocs.io/en/stable/api/efficient_did.html): Chen, Sant'Anna & Xie (2025) efficient DiD with optimal weighting for tighter SEs
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- [TROP](https://diff-diff.readthedocs.io/en/stable/api/trop.html): Triply Robust Panel estimator (Athey et al. 2025) with nuclear norm factor adjustment (absorbing by default; `non_absorbing=True` for on/off treatment, method='local')
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- [StaggeredTripleDifference](https://diff-diff.readthedocs.io/en/stable/api/staggered.html#staggeredtripledifference): Ortiz-Villavicencio & Sant'Anna (2025) staggered DDD with group-time ATT. DEPRECATED in 3.9, removed in 4.0 - use `TripleDifference` with `first_treat=` (supplying the unit id, the calendar period column and `partition=`) - the same engine (`eligibility=` is `partition=` there; `control_group` takes the underscored values). Alias `SDDD` deprecated with it
- [LPDiD](https://diff-diff.readthedocs.io/en/stable/api/lpdid.html): Dube, Girardi, Jorda & Taylor (2025) Local Projections DiD: per-horizon long-difference event study on clean controls (no negative weighting); variance- or equally-weighted ATT, premean differencing, pooled pre/post, fast. Absorbing by default; non-absorbing (reversible) treatment via `non_absorbing="first_entry"` (Eq. 12) or `"effect_stabilization"` (Eq. 13, window `L`). Complex-survey designs (pweight + stratified-PSU TSL SEs) on the default path via `fit(survey_design=...)`.
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- [ChangesInChanges](https://diff-diff.readthedocs.io/en/stable/api/changes_in_changes.html): Athey & Imbens (2006) nonlinear/distributional DiD for the 2x2 design: recovers the treated group's full counterfactual outcome distribution and quantile treatment effects (ATT + QTE grid) via the CDF transformation `F_10(F_00^{-1}(F_01(y)))`; invariant to monotone outcome transformations (unconditional fits; the covariate QR branch is not); bootstrap inference (panel or repeated cross-section resampling); point parity with R `qte::CiC()`, including its covariate branch (`covariates=` -> per-cell linear quantile regression, Melly-Santangelo-style conditional CiC). Continuous outcomes, numeric covariates. Alias `CiC`.
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- [QDiD](https://diff-diff.readthedocs.io/en/stable/api/changes_in_changes.html): **Deprecated 3.9, removed 4.0 - use `ChangesInChanges(method="qdid")`.** Athey & Imbens (2006) quantile DiD comparison estimator (additive quantile-by-quantile DiD, matching R `qte::QDiD()` including its covariate branch via `covariates=`); same bootstrap machinery as ChangesInChanges. The paper recommends CiC over QDiD (scale-dependent model with testable restrictions; a non-monotonicity warning fires when violated - unconditional fits only, the covariate-path counterfactual quantile curve is monotone by construction).
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