Did you do this? still curious about the results and think about this every now and then :)
seems so unlikely on my current models that it’ll work blinded, so if it does work this will be quite an interesting update and I’ll also have to try it out myself
You specify glucose. Have you tried small doses of sucrose/fructose/fruit and found it to not work in the same way?
Have you tried larger doses?
This is very interesting. I’m very curious to hear how the self-blinded experiment goes.
(probably not gabapentin, contrary to the name gabapentin is not actually a gabaergic. Researching it for some people I’m close to I got the impression it was kinda sketchy medication and bad risk/reward for their cases though I no longer remember specifics. I think it would not have alcohol-substitutable effects, though I haven’t taken so i could be missing something)
Hey David, I really like your paper, hadn’t seen it til now. Sorry for not doing a thorough literature review and catching it!
Super cool paper too, exciting to see. Seems like there’s a good amount of overlap in what motivated our approaches, too, though your rationale seems more detailed/rigorous/sophisticated—I’ll have to read it more thoroughly and try to absorb the generators of that process.
Then it looks like my contribution here was just making the threshold have a parameter per-feature and defining some pseudoderivatives so that threshold parameters could be learned (though I was framing it as an ‘inhibitory bias’ at the time, I now like the threshold framing)
I’ll add a citation to your paper shortly (probably this evening, though possibly tomorrow)
Wild that you did that already, ten years ago. super cool.
Thanks for commenting and letting me know! :)
Thank you!
That’s super cool you’ve been doing something similar. I’m curious to see what direction you went in. It seemed like there’s a large space of possible things to do along these lines. DeepMind also did a similar but different thing here.
What does the distribution of learned biases look like?
That’s a great question, something I didn’t note in here is that positive biases have no effect on the output of the SAE—so, if the biases were to be mostly positive that would suggest this approach is missing something. I saved histograms of the biases during training, and they generally look to be mostly (80-99% of bias values I feel like?) negative. I expect the exact distributions vary a good bit depending on L1 coefficient though.
I’ll post histograms here shortly. I also have the model weights so I can check in more detail or send you weights if you’d like either of those things.
On a related point, something I considered: since positive biases behave the same as zeros, why not use ProLU where the bias is negative and regular ReLU where the biases are positive? I tried this, and it seemed fine but it didn’t seem to make a notable impact on performance. I expect there’s some impact, but like a <5% change and I don’t know in which direction, so I stuck with the simpler approach. Plus, anyways, most of the bias values tend to be negative.
For the STE variant, did you find it better to use the STE approximation for the activation gradient, even though the approximation is only needed for the bias?
I think you’re asking whether it’s better to use the STE gradient only on the bias term, since the mul () term already has a ‘real gradient’ defined. If I’m interpreting correctly, I’m pretty sure the answer is yes. I think I tried using the synthetic grads just for the bias term and found that performed significantly worse (I’m also pretty sure I tried the reverse just in case—and that this did not work well either). I’m definitely confused on what exactly is going on with this. The derivation of these from the STE assumption is the closest thing I have to an explanation and then being like “and you want to derive both gradients from the same assumptions for some reason, so use the STE grads for too.” But this still feels pretty unsatisfying to me, especially when there’s so many degrees of freedom in deriving STE grads:
choice of STE
I glossed over this but it seems like maybe we should think of the grads of like where
I think this because for
I also see an argument from this that should be a term in the partial of , which is a property I like about taking as it’s own derivative
Another note on the STE grads: I first found these gradients worked emperically, was pretty confused by this, spent a bunch of time trying to find an intuitive explanation for them plus trying and failing to find a similar-but-more-sensible thing that works better. Then one night I realized that those exact gradient come pretty nicely from these STE assumptions, and it’s the best hypothesis I have for “why this works” but I still feel like I’m missing part of the picture.
I’d be curious if there are situations where the STE-style grads work well in a regular ReLU, but I expect not. I think it’s more that there is slack in the optimization problem induced by being unable to optimize directly for L0. I think it might be just that the STE grads with L1 regularization point more in the direction of L0 minimization. I have a little analysis I did supporting this I’ll add to the post when I get some time.
Hmm maybe I’m misunderstanding something, but I think the reason I’m disagreeing is that the losses being compared are wrt a different distribution (the ground truth actual next token) so I don’t think comparing two comparisons between two distributions is equivalent to comparing the two distributions directly.
Eg, I think for these to be the same it would need to be the case that something along the lines
or
were true, but I don’t think either of those are true. To connect that to this specific case, have be the data distribution, and and the model with and without replaced activations
on a separate note that could also be a crux,
measures how replacing activations changes the total loss of the model
quite underspecifies what “reconstruction score” is. So I’ll give a brief explanation:
let:
be the CE loss of the model unperturbed on the data distribution
be the CE loss of the model when activations are replaced with the reconstructed activations
be the CE loss of the model when activations are replaced with the zero vector
then
so, this has the property that when the value is 0 the SAE is as bad as replacement with zeros and when it’s 1 the SAE is not degrading performance at all
It’s not clear that normalizing with makes a ton of sense, but since it’s an emerging domain it’s not fully clear what metrics to use and this one is pretty standard/common. I’d prefer if bits/nats lost were the norm, but I haven’t ever seen someone use that.
I think these aren’t equivalent? KL divergence between the original model’s outputs and the outputs of the patched model is different than reconstruction loss. Reconstruction loss is the CE loss of the patched model. And CE loss is essentially the KL divergence of the prediction with the correct next token, as opposed to with the probability distribution of the original model.
Also reconstruction loss/score is in my experience the more standard metric here, though both can say something useful.
I want to mention that in my experience a factor of 2 difference in L0 makes a pretty huge difference in reconstruction score/L2 norm. IMO ideally you should compare pareto curves for each architecture or get two datapoints that have almost the exact same L0 if you want to compare two architectures.
I agree with pretty much all these points. This problem has motivated some work I have been doing and has been pretty relevant to think well about and test so I made some toy models of the situation.
This is a minimal proof of concept example I had lying around, and insufficient to prove this will happen in larger model, but definitely shows that composite features are a possible outcome and validates what you’re saying:
Here, it has not learned a single atomic feature.
All the true features are orthogonal which makes it easier to read the cosine-similarity heatmap.
and are mean and standard deviation of all features.
Note on “bias only” on the y-axis: The “bias only” entry in the learned features is the cosine similarity of the decoder bias with the ground truth features. It’s all zeros, because I disabled the bias for this run to make the decoder weights more directly interpretable. otherwise, in such a small model it’ll use the bias to do tricky things which also make the graph much less readable. We know the features are centered around the origin in this toy so zeroing the bias seems fine to do.
Edit: Remembered I have a larger example of the phenomena. Same setup as above.
This is a very interesting post to me in general and extra interesting because this may hold the key to what’s going on with some mysteriously-good-sleep I’ve been experiencing.
I recently had a couple random absurdly good nights of sleep. Like, I don’t remember feeling so energized, refreshed, healthy, good etc after a night of sleep as I did these couple nights. Two back to back nights in particular were perfect and extremely strong signal, but I think there have been a few other mornings I woke up before my alarm feeling better than expected. I have been trying and failing to figure out what caused this
the context that makes this interesting: I was in the tail end of a covid infection, and I’d been taking s-acetyl l-glutathione (SAG) and N-acetylcysteine (NAC) off and on during it (covid depletes glutathione and this is associated w/ worse outcomes). I unfortunately don’t know exactly when I was taking SAG and NAC but it would fit with the good sleep nights appearing to be happening at random since I was taking them off and on and not paying attention for any possible effect.
Anyways, this is not necessarily the explanation for my extremely good sleep nights but it’s the most likely hypothesis I have currently, still probably <30% likelihood
Thankfully I can test that hypothesis pretty clearly to my satisfaction by just taking glutathione enhancers for a week or so. The good nights of sleep were so abnormally good that getting more of them would be an extremely clear signal.
So, I expect to be testing this out this week, and I’ll try to remember to report back with the outcome.
Thanks for making this interesting post and the possible lead on what was causing the very good sleep!