Alycia Lee

Brando Miranda, Alycia Lee, Sudharsan Sundar et al.

Current trends in pre-training Large Language Models (LLMs) primarily focus on the scaling of model and dataset size. While the quality of pre-training data is considered an important factor for training powerful LLMs, it remains a nebulous concept that has not been rigorously characterized. To this end, we propose a formalization of one key aspect of data quality -- measuring the variability of natural language data -- specifically via a measure we call the diversity coefficient. Our empirical analysis shows that the proposed diversity coefficient aligns with the intuitive properties of diversity and variability, e.g., it increases as the number of latent concepts increases. Then, we measure the diversity coefficient of publicly available pre-training datasets and demonstrate that their formal diversity is high compared to theoretical lower and upper bounds. Finally, we conduct a comprehensive set of controlled interventional experiments with GPT-2 and LLaMAv2 that demonstrate the diversity coefficient of pre-training data characterizes useful aspects of downstream model evaluation performance -- totaling 44 models of various sizes (51M to 7B parameters). We conclude that our formal notion of diversity is an important aspect of data quality that captures variability and causally leads to improved evaluation performance.

Kevin K. Yang, Yuxin Chen, Alycia Lee et al.

In many high-throughput experimental design settings, such as those common in biochemical engineering, batched queries are more cost effective than one-by-one sequential queries. Furthermore, it is often not possible to directly choose items to query. Instead, the experimenter specifies a set of constraints that generates a library of possible items, which are then selected stochastically. Motivated by these considerations, we investigate \emph{Batched Stochastic Bayesian Optimization} (BSBO), a novel Bayesian optimization scheme for choosing the constraints in order to guide exploration towards items with greater utility. We focus on \emph{site-saturation mutagenesis}, a prototypical setting of BSBO in biochemical engineering, and propose a natural objective function for this problem. Importantly, we show that our objective function can be efficiently decomposed as a difference of submodular functions (DS), which allows us to employ DS optimization tools to greedily identify sets of constraints that increase the likelihood of finding items with high utility. Our experimental results show that our algorithm outperforms common heuristics on both synthetic and two real protein datasets.