缩放比例
计算机科学
水准点(测量)
推论
算法
人工智能
指纹(计算)
比例(比率)
统计物理学
签名(拓扑)
过程(计算)
扩散
模式识别(心理学)
碎片(计算)
训练集
质谱
匹配(统计)
生物系统
培训(气象学)
编码(内存)
机器学习
谱线
合成数据
数据挖掘
深度学习
作者
Montgomery Bohde,Hongxuan Liu,Mrunali Manjrekar,Magdalena Lederbauer,Shuiwang Ji,Runzhong Wang,Connor W. Coley
标识
DOI:10.48550/arxiv.2604.16648
摘要
Tandem mass spectrometry is prominent in scientific discovery workflows for identifying unknown small molecules, yet high-throughput structural elucidation remains challenging. While recent autoregressive and graph diffusion models have shown promise in de novo elucidation, performance remains limited by poor scalability during both training and inference time. In this work, we present FRIGID, a framework with a novel diffusion language model that generates molecular structures conditioned on mass spectra via intermediate fingerprint representations and determined chemical formulae, training at the scale of hundreds of millions of unlabeled structures. We then demonstrate how forward fragmentation models enable inference-time scaling by identifying spectrum-inconsistent fragments and refining them through targeted remasking and denoising. While FRIGID already achieves strong performance with its diffusion base, inference-time scaling significantly improves its accuracy, surpassing 18% Top-1 accuracy on the challenging MassSpecGym benchmark and tripling the Top-1 accuracy of the leading methods on NPLIB1. Further empirical analyses show that FRIGID exhibits log-linear performance scaling with increasing inference-time compute, opening a promising new direction for continued improvements in de novo structural elucidation. FRIGID code is publicly available at https://github.com/coleygroup/FRIGID.
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