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Neha Prasad

Publications and source records attributed to Neha Prasad.

4 recordsLinked to original sources

BioNeMo Framework: a modular, high-performance library for AI model development in drug discovery

Artificial Intelligence models encoding biology and chemistry are opening new routes to high-throughput and high-quality in-silico drug development. However, their training increasingly relies on computational scale, with recent protein language models (pLM) training on hundreds of graphical processing units (GPUs). We introduce the BioNeMo Framework to facilitate the training of computational biology and chemistry AI models across hundreds of GPUs. Its modular design allows the integration of individual components, such as data loaders, into existing workflows and is open to community contributions. We detail technical features of the BioNeMo Framework through use cases such as pLM pre-training and fine-tuning. On 256 NVIDIA A100s, BioNeMo Framework trains a three billion parameter BERT-based pLM on over one trillion tokens in 4.2 days. The BioNeMo Framework is open-source and free for everyone to use.

cs.LG

The DeCAMFounder: Non-Linear Causal Discovery in the Presence of Hidden Variables

Many real-world decision-making tasks require learning causal relationships between a set of variables. Traditional causal discovery methods, however, require that all variables are observed, which is often not feasible in practical scenarios. Without additional assumptions about the unobserved variables, it is not possible to recover any causal relationships from observational data. Fortunately, in many applied settings, additional structure among the confounders can be expected. In particular, pervasive confounding is commonly encountered and has been utilized for consistent causal estimation in linear causal models. In this paper, we present a provably consistent method to estimate causal relationships in the non-linear, pervasive confounding setting. The core of our procedure relies on the ability to estimate the confounding variation through a simple spectral decomposition of the observed data matrix. We derive a DAG score function based on this insight, prove its consistency in recovering a correct ordering of the DAG, and empirically compare it to previous approaches. We demonstrate improved performance on both simulated and real datasets by explicitly accounting for both confounders and non-linear effects.

stat.ME

Transfer Learning with Kernel Methods

Transfer learning refers to the process of adapting a model trained on a source task to a target task. While kernel methods are conceptually and computationally simple machine learning models that are competitive on a variety of tasks, it has been unclear how to perform transfer learning for kernel methods. In this work, we propose a transfer learning framework for kernel methods by projecting and translating the source model to the target task. We demonstrate the effectiveness of our framework in applications to image classification and virtual drug screening. In particular, we show that transferring modern kernels trained on large-scale image datasets can result in substantial performance increase as compared to using the same kernel trained directly on the target task. In addition, we show that transfer-learned kernels allow a more accurate prediction of the effect of drugs on cancer cell lines. For both applications, we identify simple scaling laws that characterize the performance of transfer-learned kernels as a function of the number of target examples. We explain this phenomenon in a simplified linear setting, where we are able to derive the exact scaling laws. By providing a simple and effective transfer learning framework for kernel methods, our work enables kernel methods trained on large datasets to be easily adapted to a variety of downstream target tasks.

cs.LG

Optimal Transport using GANs for Lineage Tracing

In this paper, we present Super-OT, a novel approach to computational lineage tracing that combines a supervised learning framework with optimal transport based on Generative Adversarial Networks (GANs). Unlike previous approaches to lineage tracing, Super-OT has the flexibility to integrate paired data. We benchmark Super-OT based on single-cell RNA-seq data against Waddington-OT, a popular approach for lineage tracing that also employs optimal transport. We show that Super-OT achieves gains over Waddington-OT in predicting the class outcome of cells during differentiation, since it allows the integration of additional information during training.

cs.LG