Single-cell transcriptomics enabled the study of cellular heterogeneity in response to perturbations at the resolution of individual cells. However, scaling high-throughput screens (HTSs) to measure cellular responses for many drugs remains a challenge due to technical limitations and, more importantly, the cost of such multiplexed experiments. Thus, transferring information from routinely performed bulk RNA HTS is required to enrich single-cell data meaningfully. We introduce chemCPA, a new encoder-decoder architecture to study the perturbational effects of unseen drugs. We combine the model with an architecture surgery for transfer learning and demonstrate how training on existing bulk RNA HTS datasets can improve generalisation performance. Better generalisation reduces the need for extensive and costly screens at single-cell resolution. We envision that our proposed method will facilitate more efficient experiment designs through its ability to generate in-silico hypotheses, ultimately accelerating drug discovery.
翻译:单细胞转基因组学有助于针对个别细胞解析时的扰动作用研究细胞异质性。然而,由于技术限制,而且更重要的是,这种多轴实验的成本,由于这种技术限制,从例行进行的大型RNA HTS中传输信息,才能有意义地丰富单细胞数据。我们引进了一种新的化学化学化学共振器,这是一种研究隐形药物的扰动效应的新的编码器解码器结构。我们将该模型与用于转移学习的建筑外科手术结合起来,并演示如何对现有成批RNA HTS数据集的培训可以改善一般化性能。更好的概括化减少了单细胞分辨率对广泛和昂贵的屏幕的需求。我们设想,我们拟议的方法将促进更有效的实验设计,因为它能够产生硅假体的假体,最终加速药物的发现。