4.7 Article

scDLC: a deep learning framework to classify large sample single-cell RNA-seq data

期刊

BMC GENOMICS
卷 23, 期 1, 页码 -

出版社

BMC
DOI: 10.1186/s12864-022-08715-1

关键词

Single-cell RNA sequencing; Deep learning; Classifier

资金

  1. National Natural Science Foundation of China [1207010822, 12071305, 11871390, 11871411, 11731011]
  2. Natural Science Foundation of Guangdong Province of China [2020B1515310008]
  3. Project of Educational Commission of Guangdong Province of China [2019KZDZX1007]
  4. General Research Fund [HKBU12303918]
  5. Initiation Grant for Faculty Niche Research Areas of Hong Kong Baptist University [RC-FNRA-IG/20-21/SCI/03]

向作者/读者索取更多资源

In this study, a new deep learning classifier is proposed for large sample scRNA-seq data. The classifier outperforms existing methods in various settings and does not require prior knowledge of the data distribution.
Background: Using single-cell RNA sequencing (scRNA-seq) data to diagnose disease is an effective technique in medical research. Several statistical methods have been developed for the classification of RNA sequencing (RNA-seq) data, including, for example, Poisson linear discriminant analysis (PLDA), negative binomial linear discriminant analysis (NBLDA), and zero-inflated Poisson logistic discriminant analysis (ZIPLDA). Nevertheless, few existing methods perform well for large sample scRNA-seq data, in particular when the distribution assumption is also violated. Results: We propose a deep learning classifier (scDLC) for large sample scRNA-seq data, based on the long short-term memory recurrent neural networks (LSTMs). Our new scDLC does not require a prior knowledge on the data distribution, but instead, it takes into account the dependency of the most outstanding feature genes in the LSTMs model. LSTMs is a special recurrent neural network, which can learn long-term dependencies of a sequence. Conclusions: Simulation studies show that our new scDLC performs consistently better than the existing methods in a wide range of settings with large sample sizes. Four real scRNA-seq datasets are also analyzed, and they coincide with the simulation results that our new scDLC always performs the best. The code named scDLC is publicly available at https://github.com/scDLC-code/code.

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