TY - JOUR
T1 - scDLC
T2 - a deep learning framework to classify large sample single-cell RNA-seq data
AU - Zhou, Yan
AU - Peng, Minjiao
AU - Yang, Bin
AU - Tong, Tiejun
AU - Zhang, Baoxue
AU - Tang, Niansheng
N1 - Yan Zhou’s research was supported by the National Natural Science Foundation of China (Grant No. 12071305, 11871390 and 11871411), Natural Science Foundation of Guangdong Province of China under grant 2020B1515310008, Project of Educational Commission of Guangdong Province of China under grant 2019KZDZX1007. Niansheng Tang’s research was supported by the National Natural Science Foundation of China (Grant No. 11731011). Tiejun Tong’s research was supported by the General Research Fund (HKBU12303918), the National Natural Science Foundation of China (1207010822), and the Initiation Grant for Faculty Niche Research Areas (RC-FNRA-IG/20-21/SCI/03) of Hong Kong Baptist University.
Publisher Copyright:
© 2022, The Author(s).
PY - 2022/12
Y1 - 2022/12
N2 - 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.
AB - 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.
KW - Classifier
KW - Deep learning
KW - Single-cell RNA sequencing
UR - http://www.scopus.com/inward/record.url?scp=85133990718&partnerID=8YFLogxK
U2 - 10.1186/s12864-022-08715-1
DO - 10.1186/s12864-022-08715-1
M3 - Journal article
C2 - 35831808
AN - SCOPUS:85133990718
SN - 1471-2164
VL - 23
JO - BMC Genomics
JF - BMC Genomics
IS - 1
M1 - 504
ER -