Evidence map›Paper›PMID 35831808›Full record

ArticleBMC genomics2022

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

Yan Zhou, Minjiao Peng, Bin Yang, Tiejun Tong, Baoxue Zhang, Niansheng Tang

Abstract read
In one paragraph

Article in BMC genomics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Article
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  4. Frontiers in immunology · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Yan ZhouCollege of Mathematics and Statistics, Institute of Statistical Sciences, Shenzhen Key Laboratory of Advanced Machine Learning and Applications, Shenzhen University, Shenzhen, China.
Minjiao PengCollege of Mathematics and Statistics, Institute of Statistical Sciences, Shenzhen Key Laboratory of Advanced Machine Learning and Applications, Shenzhen University, Shenzhen, China.
Bin YangCollege of Mathematics and Statistics, Institute of Statistical Sciences, Shenzhen Key Laboratory of Advanced Machine Learning and Applications, Shenzhen University, Shenzhen, China.
Tiejun TongDepartment of Mathematics, Hong Kong Baptist University, Kowloon Tong, Hong Kong.
Baoxue ZhangSchool of Statistics, Capital University of Economics and Business, Beijing, China.
Niansheng TangYunnan Key Laboratory of Statistical Modeling and Data Analysis, Yunnan University, Kunming, China. nstang@ynu.edu.cn.

Funding

Initiation Grant for Faculty Niche Research Areas of Hong Kong Baptist University RC-FNRA-IG/20-21/SCI/03National Natural Science Foundation of China 11731011National Natural Science Foundation of China 12071305, 11871390 , 11871411 and 1207010822Natural Science Foundation of Guangdong Province of China 2020B1515310008Project of Educational Commission of Guangdong Province of China 2019KZDZX1007the General Research Fund HKBU12303918
6 · The paper itself

Abstract

backgroundUsing 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.

resultsWe 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.

conclusionsSimulation 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 .

Indexed as

Deep LearningDiscriminant AnalysisGene Expression ProfilingRNARNA-SeqSequence Analysis, RNASingle-Cell AnalysisRNAClassifierDeep learningSingle-cell RNA sequencing

Identifiers

PMID35831808
PMCPMC9281153

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.