Author:
Dincer Ayse Berceste,Celik Safiye,Hiranuma Naozumi,Lee Su-In
Abstract
AbstractWe present the DeepProfile framework, which learns a variational autoencoder (VAE) network from thousands of publicly available gene expression samples and uses this network to encode a low-dimensional representation (LDR) to predict complex disease phenotypes. To our knowledge, DeepProfile is the first attempt to use deep learning to extract a feature representation from a vast quantity of unlabeled (i.e, lacking phenotype information) expression samples that are not incorporated into the prediction problem. We use Deep-Profile to predict acute myeloid leukemia patients’ in vitro responses to 160 chemotherapy drugs. We show that, when compared to the original features (i.e., expression levels) and LDRs from two commonly used dimensionality reduction methods, DeepProfile: (1) better predicts complex phenotypes, (2) better captures known functional gene groups, and (3) better reconstructs the input data. We show that DeepProfile is generalizable to other diseases and phenotypes by using it to predict ovarian cancer patients’ tumor invasion patterns and breast cancer patients’ disease subtypes.
Publisher
Cold Spring Harbor Laboratory
Reference22 articles.
1. The cancer cell line encyclopedia enables predictive mod-elling of anticancer drug sensitivity;Nature,2012
2. Extracting a low-dimensional description of multiple gene expression datasets reveals a potential driver for tumor-associated stroma in ovarian cancer;Genome Medicine,2016
3. Chiu, Y. , Chen, H. H. , Zhang, T. , Zhang, S. , Gorthi, A. , Wang, L. , Huang, Y. , and Chen, Y. Predicting drug response of tumors from integrated genomic profiles by deep neural networks. arXiv preprint arXiv:1805.07702, 2018.
4. A community effort to assess and improve drug sensitivity prediction algorithms
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