| Literature DB >> 33153777 |
Zhenyu Wu1, Patrick J Lawrence1, Anjun Ma1, Jian Zhu2, Dong Xu3, Qin Ma4.
Abstract
Rapidly developing single-cell sequencing analyses produce more comprehensive profiles of the genomic, transcriptomic, and epigenomic heterogeneity of tumor subpopulations than do traditional bulk sequencing analyses. Moreover, single-cell techniques allow the response of a tumor to drug exposure to be more thoroughlyinvestigated. Deep learning (DL) models have successfully extracted features from complex bulk sequence data to predict drug responses. We review recent innovations in single-cell technologies and DL-based approaches related to drug sensitivity predictions. We believe that, by using insights from bulk sequencedata, deep transfer learning (DTL) can facilitate the use of single-cell data for training superior DL-based drug prediction models.Entities:
Keywords: deep learning models; deep transfer learning framework; drug response; single-cell technologies
Year: 2020 PMID: 33153777 PMCID: PMC7669610 DOI: 10.1016/j.tips.2020.10.004
Source DB: PubMed Journal: Trends Pharmacol Sci ISSN: 0165-6147 Impact factor: 14.819