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dc.contributor.authorZhang, X.
dc.contributor.authorChen, Z.
dc.contributor.authorBhadani, R.
dc.contributor.authorCao, S.
dc.contributor.authorLu, M.
dc.contributor.authorLytal, N.
dc.contributor.authorChen, Y.
dc.contributor.authorAn, L.
dc.date.accessioned2022-08-01T20:18:17Z
dc.date.available2022-08-01T20:18:17Z
dc.date.issued2022
dc.identifier.citationZhang, X., Chen, Z., Bhadani, R., Cao, S., Lu, M., Lytal, N., Chen, Y., & An, L. (2022). NISC: Neural Network-Imputation for Single-Cell RNA Sequencing and Cell Type Clustering. Frontiers in Genetics, 13.
dc.identifier.issn1664-8021
dc.identifier.doi10.3389/fgene.2022.847112
dc.identifier.urihttp://hdl.handle.net/10150/665487
dc.description.abstractSingle-cell RNA sequencing (scRNA-seq) reveals the transcriptome diversity in heterogeneous cell populations as it allows researchers to study gene expression at single-cell resolution. The latest advances in scRNA-seq technology have made it possible to profile tens of thousands of individual cells simultaneously. However, the technology also increases the number of missing values, i. e, dropouts, from technical constraints, such as amplification failure during the reverse transcription step. The resulting sparsity of scRNA-seq count data can be very high, with greater than 90% of data entries being zeros, which becomes an obstacle for clustering cell types. Current imputation methods are not robust in the case of high sparsity. In this study, we develop a Neural Network-based Imputation for scRNA-seq count data, NISC. It uses autoencoder, coupled with a weighted loss function and regularization, to correct the dropouts in scRNA-seq count data. A systematic evaluation shows that NISC is an effective imputation approach for handling sparse scRNA-seq count data, and its performance surpasses existing imputation methods in cell type identification. Copyright © 2022 Zhang, Chen, Bhadani, Cao, Lu, Lytal, Chen and An.
dc.language.isoen
dc.publisherFrontiers Media S.A.
dc.rightsCopyright © 2022 Zhang, Chen, Bhadani, Cao, Lu, Lytal, Chen and An. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
dc.rights.urihttps://creativecommons.org/licenses/by/4.0
dc.subjectautoencoder
dc.subjectdeep learning
dc.subjectdropout
dc.subjectimputation
dc.subjectsingle cell RNA-seq
dc.titleNISC: Neural Network-Imputation for Single-Cell RNA Sequencing and Cell Type Clustering
dc.typeArticle
dc.typetext
dc.contributor.departmentInterdisciplinary Program in Statistics and Data Science, University of Arizona
dc.contributor.departmentDepartment of Biosystems Engineering, University of Arizona
dc.contributor.departmentDepartment of Electrical and Computer Engineering, University of Arizona
dc.contributor.departmentCollege of Pharmacy, University of Arizona
dc.contributor.departmentDepartment of Biostatistics and Epidemiology, University of Arizona
dc.identifier.journalFrontiers in Genetics
dc.description.noteOpen access journal
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal published version
dc.source.journaltitleFrontiers in Genetics
refterms.dateFOA2022-08-01T20:18:17Z


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Copyright © 2022 Zhang, Chen, Bhadani, Cao, Lu, Lytal, Chen and An. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).
Except where otherwise noted, this item's license is described as Copyright © 2022 Zhang, Chen, Bhadani, Cao, Lu, Lytal, Chen and An. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY).