DeepImpute: an accurate, fast and scalable deep neural network method to impute single-cell RNA-Seq data

Author:

Arisdakessian Cedric,Poirion Olivier,Yunits Breck,Zhu Xun,Garmire Lana X.

Abstract

BackgroundSingle-cell RNA sequencing (scRNA-seq) offers new opportunities to study gene expression of tens of thousands of single cells simultaneously. However, a significant problem of current scRNA-seq data is the large fractions of missing values or “dropouts” in gene counts. Incorrect handling of dropouts may affect downstream bioinformatics analysis. As the number of scRNA-seq datasets grows drastically, it is crucial to have accurate and efficient imputation methods to handle these dropouts.MethodsWe present DeepImpute, a deep neural network based imputation algorithm. The architecture of DeepImpute efficiently uses dropout layers and loss functions to learn patterns in the data, allowing for accurate imputation.ResultsOverall DeepImpute yields better accuracy than other publicly available scRNA-Seq imputation methods on experimental data, as measured by mean squared error or Pearson’s correlation coefficient. Moreover, its efficient implementation provides significantly higher performance over the other methods as dataset size increases. Additionally, as a machine learning method, DeepImpute allows to use a subset of data to train the model and save even more computing time, without much sacrifice on the prediction accuracy.ConclusionsDeepImpute is an accurate, fast and scalable imputation tool that is suited to handle the ever increasing volume of scRNA-seq data. The package is freely available at https://github.com/lanagarmire/DeepImpute

Publisher

Cold Spring Harbor Laboratory

Reference43 articles.

1. Abadi,M. et al. (2016) TensorFlow: A System for Large-Scale Machine Learning. In, OSDI., pp.265–283.

2. Deep Learning Accurately Predicts Estrogen Receptor Status in Breast Cancer;Metabolomics Data. J. Proteome Res.,2018

3. Andrews,T.S. and Hemberg,M. (2016) Modelling dropouts allows for unbiased identification of marker genes in scRNASeq experiments. bioRxiv, 065094.

4. MISSING DATA IMPUTATION IN THE ELECTRONIC HEALTH RECORD USING DEEPLY LEARNED AUTOENCODERS;Pac. Symp. Biocomput,2017

Cited by 9 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3