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      McImpute: Matrix Completion Based Imputation for Single Cell RNA-seq Data

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          Abstract

          Motivation: Single-cell RNA sequencing has been proved to be revolutionary for its potential of zooming into complex biological systems. Genome-wide expression analysis at single-cell resolution provides a window into dynamics of cellular phenotypes. This facilitates the characterization of transcriptional heterogeneity in normal and diseased tissues under various conditions. It also sheds light on the development or emergence of specific cell populations and phenotypes. However, owing to the paucity of input RNA, a typical single cell RNA sequencing data features a high number of dropout events where transcripts fail to get amplified.

          Results: We introduce mcImpute, a low-rank matrix completion based technique to impute dropouts in single cell expression data. On a number of real datasets, application of mcImpute yields significant improvements in the separation of true zeros from dropouts, cell-clustering, differential expression analysis, cell type separability, the performance of dimensionality reduction techniques for cell visualization, and gene distribution.

          Availability and Implementation: https://github.com/aanchalMongia/McImpute_scRNAseq

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          Most cited references36

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          Exact Matrix Completion via Convex Optimization

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            Reference component analysis of single-cell transcriptomes elucidates cellular heterogeneity in human colorectal tumors

            Shyam Prabhakar, Paul Robson, Iain Beehuat Tan and colleagues characterize the cellular heterogeneity of colorectal tumors and their microenvironment on the basis of single-cell RNA–seq data analyzed with their newly developed clustering algorithm, reference component analysis (RCA). Their analyses identify two subtypes of cancer-associated fibroblasts and further divide tumors into subgroups with divergent survival probabilities.
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              The Power of Convex Relaxation: Near-Optimal Matrix Completion

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                Author and article information

                Contributors
                Journal
                Front Genet
                Front Genet
                Front. Genet.
                Frontiers in Genetics
                Frontiers Media S.A.
                1664-8021
                29 January 2019
                2019
                : 10
                : 9
                Affiliations
                [1] 1Department of Computer Science and Engineering, Indraprastha Institute of Information Technology Delhi , New Delhi, India
                [2] 2Center for Computational Biology, Indraprastha Institute of Information Technology Delhi , New Delhi, India
                [3] 3Department of Electronics and Communications Engineering, Indraprastha Institute of Information Technology Delhi , New Delhi, India
                Author notes

                Edited by: Indrajit Saha, National Institute of Technical Teachers' Training and Research, India

                Reviewed by: Kumardeep Chaudhary, Icahn School of Medicine at Mount Sinai, United States; Sumit Kumar Bag, National Botanical Research Institute (CSIR), India; Yuriy L. Orlov, Russian Academy of Sciences, Russia; Shaoli Das, National Institutes of Health (NIH), United States

                *Correspondence: Debarka Sengupta debarka@ 123456iiitd.ac.in

                This article was submitted to Bioinformatics and Computational Biology, a section of the journal Frontiers in Genetics

                Article
                10.3389/fgene.2019.00009
                6361810
                30761179
                1b0a5eb2-6e5f-4910-832d-6a1cbbf0ff2b
                Copyright © 2019 Mongia, Sengupta and Majumdar.

                This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

                History
                : 08 August 2018
                : 10 January 2019
                Page count
                Figures: 7, Tables: 0, Equations: 0, References: 53, Pages: 12, Words: 7379
                Categories
                Genetics
                Original Research

                Genetics
                scrna-seq,dropouts,imputation,matrix completion,nuclear norm minization
                Genetics
                scrna-seq, dropouts, imputation, matrix completion, nuclear norm minization

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