PBLR: an accurate single cell RNA-seq data imputation tool considering cell heterogeneity and prior expression level of dropouts
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[1] Mark Crovella,et al. Targeted matrix completion , 2017, SDM.
[2] Kathryn Roeder,et al. A United Statistical Framework for Single Cell and Bulk Sequencing Data , 2016, bioRxiv.
[3] R. Sandberg,et al. Single-Cell RNA-Seq Reveals Dynamic, Random Monoallelic Gene Expression in Mammalian Cells , 2014, Science.
[4] Shiqian Ma,et al. Fixed point and Bregman iterative methods for matrix rank minimization , 2009, Math. Program..
[5] B. Mercier,et al. A dual algorithm for the solution of nonlinear variational problems via finite element approximation , 1976 .
[6] Andrew J Rennekamp,et al. Toward a Choate View of Fate , 2018, Cell.
[7] Emmanuel J. Candès,et al. Exact Matrix Completion via Convex Optimization , 2008, Found. Comput. Math..
[8] Tal Nawy,et al. Single-cell sequencing , 2013, Nature Methods.
[9] Wei Vivian Li,et al. An accurate and robust imputation method scImpute for single-cell RNA-seq data , 2018, Nature Communications.
[10] Xiaoming Yuan,et al. Matrix completion via an alternating direction method , 2012 .
[11] S. Linnarsson,et al. Cell types in the mouse cortex and hippocampus revealed by single-cell RNA-seq , 2015, Science.
[12] A. Oudenaarden,et al. Validation of noise models for single-cell transcriptomics , 2014, Nature Methods.
[13] Bo Wang,et al. Visualization and analysis of single-cell RNA-seq data by kernel-based similarity learning , 2016, Nature Methods.
[14] N. Neff,et al. Dissecting direct reprogramming from fibroblast to neuron using single-cell RNA-seq , 2016, Nature.
[15] Philip M. Kim,et al. Subsystem identification through dimensionality reduction of large-scale gene expression data. , 2003, Genome research.
[16] Guocheng Yuan,et al. GiniClust: detecting rare cell types from single-cell gene expression data with Gini index , 2016, Genome Biology.
[17] Hannah A. Pliner,et al. Reversed graph embedding resolves complex single-cell trajectories , 2017, Nature Methods.
[18] Emmanuel J. Candès,et al. A Singular Value Thresholding Algorithm for Matrix Completion , 2008, SIAM J. Optim..
[19] Il-Youp Kwak,et al. DrImpute: imputing dropout events in single cell RNA sequencing data , 2017, BMC Bioinformatics.
[20] Nancy R. Zhang,et al. SAVER: Gene expression recovery for single-cell RNA sequencing , 2018, Nature Methods.
[21] R. Glowinski,et al. Augmented Lagrangian and Operator-Splitting Methods in Nonlinear Mechanics , 1987 .
[22] Lihua Zhang,et al. Comparison of Computational Methods for Imputing Single-Cell RNA-Sequencing Data , 2020, IEEE/ACM Transactions on Computational Biology and Bioinformatics.
[23] A. Regev,et al. Spatial reconstruction of single-cell gene expression data , 2015 .
[24] R. Glowinski,et al. Numerical Methods for Nonlinear Variational Problems , 1985 .
[25] Pablo Tamayo,et al. Metagenes and molecular pattern discovery using matrix factorization , 2004, Proceedings of the National Academy of Sciences of the United States of America.
[26] Sandhya Prabhakaran,et al. Dirichlet Process Mixture Model for Correcting Technical Variation in Single-Cell Gene Expression Data , 2016, ICML.
[27] S. Quake,et al. A survey of human brain transcriptome diversity at the single cell level , 2015, Proceedings of the National Academy of Sciences.
[28] Daphne M. Tsoucas,et al. GiniClust2: a cluster-aware, weighted ensemble clustering method for cell-type detection , 2018, Genome Biology.
[29] A. Oshlack,et al. Splatter: simulation of single-cell RNA sequencing data , 2017, Genome Biology.
[30] Haesun Park,et al. SymNMF: nonnegative low-rank approximation of a similarity matrix for graph clustering , 2014, Journal of Global Optimization.
[31] Ruiqiang Li,et al. Single-cell RNA-Seq profiling of human preimplantation embryos and embryonic stem cells , 2013, Nature Structural &Molecular Biology.
[32] P. Kharchenko,et al. Bayesian approach to single-cell differential expression analysis , 2014, Nature Methods.
[33] Alex A. Pollen,et al. Low-coverage single-cell mRNA sequencing reveals cellular heterogeneity and activated signaling pathways in developing cerebral cortex , 2014, Nature Biotechnology.
[34] Guo-Cheng Yuan,et al. A cluster-aware, weighted ensemble clustering method for cell-type detection , 2018 .
[35] M. Schaub,et al. SC3 - consensus clustering of single-cell RNA-Seq data , 2016, Nature Methods.
[36] E. Candès,et al. Exact low-rank matrix completion via convex optimization , 2008, 2008 46th Annual Allerton Conference on Communication, Control, and Computing.
[37] Sara Ballouz,et al. Characterizing the replicability of cell types defined by single cell RNA-sequencing data using MetaNeighbor , 2018, Nature Communications.
[38] Muhammad Tayyab Asif,et al. Low-dimensional models for missing data imputation in road networks , 2013, 2013 IEEE International Conference on Acoustics, Speech and Signal Processing.
[39] N. Neff,et al. Reconstructing lineage hierarchies of the distal lung epithelium using single cell RNA-seq , 2014, Nature.
[40] Kevin R. Moon,et al. Recovering Gene Interactions from Single-Cell Data Using Data Diffusion , 2018, Cell.
[41] M. Gerstein,et al. RNA-Seq: a revolutionary tool for transcriptomics , 2009, Nature Reviews Genetics.