Goodman-Bacon decomposition
Table of contents
This section will walk you through the basic logic of Andrew
Goodman-Bacon’s TWFE decomposition. It draws upon his 2021 Journal of
Econometrics paper,
Difference-in-differences with variation in treatment
timing.
We’ll make use of the following R packages.
# install.packages(c("ggplot2", "fixest", "bacondecomp"))
library(ggplot2)
library(fixest)
library(bacondecomp)
# Optional: custom ggplot2 theme
theme_set(
theme_linedraw() +
theme(
panel.grid.minor = element_line(linetype = 3, linewidth = 0.1),
panel.grid.major = element_line(linetype = 3, linewidth = 0.1)
)
)
What is the Goodman-Bacon decomposition?
As discussed at the end of the TWFE section, the introduction of differential treatment timing makes it hard to draw a bright line between pre and post treatment periods. Let’s continue with the same dataset that we were using in the final example from that section.
dat4 = data.frame(
id = rep(1:3, times = 10),
tt = rep(1:10, each = 3)
) |>
within({
D = (id == 2 & tt >= 5) | (id == 3 & tt >= 8)
btrue = ifelse(D & id == 3, 4, ifelse(D & id == 2, 2, 0))
y = id + 1 * tt + btrue * D
})
In plot form:
ggplot(dat4, aes(x = tt, y = y, col = factor(id))) +
geom_point() + geom_line() +
geom_vline(xintercept = c(4.5, 7.5), lty = 2) +
scale_x_continuous(breaks = scales::pretty_breaks()) +
labs(x = "Time variable", y = "Outcome variable", col = "ID")
Here we see that our simulation includes two distinct treatment periods. The first treatment occurs to period 5, where id=2’s trendline jumps by 2 units. The second treatment occurs in period 8, where id=3’s trendline jumps by 4 units. In contrast, id=1 remains untreated for the duration of the experiment.
Stepping back, it’s not immediately clear how to calculate the ATT. For example, how should the late treated unit (id=3) regard the early treated unit (id=2)? Can the latter be used as control group for the former? After all, they didn’t receive treatment at the same time… but, on the other hand, id=2’s path was already altered by the initial treatment wave.
To unravel this conundrum, let’s start by estimating a simple TWFE model.
feols(y ~ D | id + tt, dat4)
OLS estimation, Dep. Var.: y
Observations: 30
Fixed-effects: id: 3, tt: 10
Standard-errors: Clustered (id)
Estimate Std. Error t value Pr(>|t|)
DTRUE 2.90909 0.725719 4.00856 0.056967 .
---
Signif. codes: 0 '***' 0.001 '**' 0.01 '*' 0.05 '.' 0.1 ' ' 1
RMSE: 0.35505 Adj. R2: 0.986455
Within R2: 0.831169
What does the resulting coefficient estimate of \(\hat{\beta}=2.91\) represent? The short answer is that it comprises a weighted average of four distinct 2x2 groups (or comparisons):
- treated vs untreated 1) early treated (\(T^e\)) vs untreated (\(U\)) 2) late treated (\(T^l\)) vs untreated (\(U\))
- differentially treated 1) early treated (\(T^e\)) vs late control (\(C^l\)) 2) late treated (\(T^l\)) vs early control (\(C^e\))
We can visualize these four comparison sets as follows:
rbind(
dat4 |> subset(id %in% c(1,2)) |> transform(role = ifelse(id==2, "Treatment", "Control"), comp = "1.1. Early vs Untreated"),
dat4 |> subset(id %in% c(1,3)) |> transform(role = ifelse(id==3, "Treatment", "Control"), comp = "1.2. Late vs Untreated"),
dat4 |> subset(id %in% c(2,3) & tt<8) |> transform(role = ifelse(id==2, "Treatment", "Control"), comp = "2.1. Early vs Untreated"),
dat4 |> subset(id %in% c(2:3) & tt>4) |> transform(role = ifelse(id==3, "Treatment", "Control"), comp = "2.2. Late vs Untreated")
) |>
ggplot(aes(tt, y, group = id, col = factor(id), lty = role)) +
geom_point() + geom_line() +
facet_wrap(~comp) +
scale_x_continuous(breaks = scales::pretty_breaks()) +
scale_linetype_manual(values = c("Control" = 5, "Treatment" = 1)) +
labs(x = "Time variable", y = "Ouroleome variable", col = "ID", lty = "Role")
In other words, the panel IDs are split into different timing cohorts based on when the first treatment takes place and where it lies in relation to the treatment of other panel IDs. The more panel IDs and differential treatment timings there are, the more the combinations of the above groups.
The Goodman-Bacon decomposition isolates each of these 2x2 comparisons and assigns them a weight, based on their relative coverage in the data (i.e., how long each comparison lasts relative to the overall timespan, and how many units were involved).
To implement the Goodman-Bacon decomposition in R, we need simply call
the bacon()
function from the bacondecomp package. An introductory
vignette to package is available
here,
although the arguments are pretty self-explanatory. Let’s see what it
yields for our present problem:
(bgd = bacon(y ~ D, dat4, id_var = "id", time_var = "tt"))
treated untreated estimate weight type
2 5 Inf 2 0.3636364 Treated vs Untreated
3 8 Inf 4 0.3181818 Treated vs Untreated
6 8 5 4 0.1363636 Later vs Earlier Treated
8 5 8 2 0.1818182 Earlier vs Later Treated
Here we get our weights and the 2x2 \(\beta\) for each group. The table tells us that (\(T\) vs \(U\)), which is the sum of the late and early treated versus never treated, has the largest weight, followed by early vs late treated, and lastly, late vs early treated.
Importantly, note that the weighted mean of these estimates is exactly the same as our earlier (naive) TWFE coefficient estimate. Again, this shouldn’t be surprising, since the whole point of the Bacon-Goodman exercise is to decompose the makeup of that estimate and thus highlight potential sources of bias.
(bgd_wm = weighted.mean(bgd$estimate, bgd$weight))
[1] 2.909091
We can easily plot this result to visualize how the different components are affecting the overall estimate.
ggplot(bgd, aes(x = weight, y = estimate, shape = type, col = type)) +
geom_hline(yintercept = bgd_wm, lty = 2) +
geom_point(size = 3) +
labs(
x = "Weight", y = "Estimate", shape = "Type", col = "Type",
title = "Bacon-Goodman decomposition example",
caption = "Note: The horizontal dotted line depicts the full TWFE estimate."
)
The figure shows four points for the four groups in our example.
- Earlier vs Later Treated (red circle).
- Later vs Earlier Treated (green triangle).
- Treated vs Untreated (two blue squares; one for the earlier treated group and another for the later treated group).
Finally, Note that the estimate values of 2 and 4 coincide with the treatment effects that were encoded into our simulation. Specifically, unit id=2 increases by 2 and unit id=3 increases by 4 over the untreated unit id=1.
So where do TWFE regressions go wrong?
TO BE COMPLETED