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Open AccessJournal ArticleDOI

SwarnSeq: An improved statistical approach for differential expression analysis of single-cell RNA-seq data.

TLDR
SwarnSeq as mentioned in this paper is an improved method for DE, and other downstream analysis that considers the molecular capture process in scRNA-seq data modeling, which has improved performance over the 11 existing methods.
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This article is published in Genomics.The article was published on 2021-03-01 and is currently open access. It has received 7 citations till now. The article focuses on the topics: Data modeling.

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Journal ArticleDOI

Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose–response study designs

TL;DR: To benchmark DGEA methods for dose–response scRNAseq experiments, a multiplicity corrected Bayesian testing approach is proposed and compared against 8 other methods including two frequentist fit-for-purpose tests using simulated and experimental data.
Journal ArticleDOI

Differential Expression Analysis of Single-Cell RNA-Seq Data: Current Statistical Approaches and Outstanding Challenges

Samarendra Das, +2 more
- 01 Jul 2022 - 
TL;DR: The underlying statistical principles of the differential expression analysis approaches are critically discussed and distinctly divide them into six major classes, i.e., generalized linear, generalized additive, Hurdle, mixture models, two-class parametric, and non-parametric approaches.
Posted ContentDOI

Benchmarking of a Bayesian single cell RNAseq differential gene expression test for dose-response study designs.

TL;DR: In this article, the authors proposed a multiplicity corrected Bayesian testing approach and compared it with 8 other methods including two frequentist fit-for-purpose tests using simulated and experimental data.
Journal ArticleDOI

Statistical Methods for Analysis of single-cell RNA-sequencing Data

TL;DR: In this paper, a novel statistical approach for various analyses of the scRNA-seq Unique Molecular Identifier (UMI) counts data is presented, which considers the biological process that leads to severe dropout events in modeling the observed UMI counts of the genes.
Journal ArticleDOI

UIPBC: An effective clustering for scRNA-seq data analysis without user input

TL;DR: Wadhury et al. as mentioned in this paper proposed an effective clustering method, which integrates required preprocessing steps for data cleaning, followed by robust cell group identification method from scRNA-seq data.
References
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Journal ArticleDOI

Moderated estimation of fold change and dispersion for RNA-seq data with DESeq2

TL;DR: This work presents DESeq2, a method for differential analysis of count data, using shrinkage estimation for dispersions and fold changes to improve stability and interpretability of estimates, which enables a more quantitative analysis focused on the strength rather than the mere presence of differential expression.
Journal ArticleDOI

edgeR: a Bioconductor package for differential expression analysis of digital gene expression data.

TL;DR: EdgeR as mentioned in this paper is a Bioconductor software package for examining differential expression of replicated count data, which uses an overdispersed Poisson model to account for both biological and technical variability and empirical Bayes methods are used to moderate the degree of overdispersion across transcripts, improving the reliability of inference.
Journal ArticleDOI

limma powers differential expression analyses for RNA-sequencing and microarray studies

TL;DR: The philosophy and design of the limma package is reviewed, summarizing both new and historical features, with an emphasis on recent enhancements and features that have not been previously described.
Journal ArticleDOI

Differential expression analysis for sequence count data.

Simon Anders, +1 more
- 27 Oct 2010 - 
TL;DR: A method based on the negative binomial distribution, with variance and mean linked by local regression, is proposed and an implementation, DESeq, as an R/Bioconductor package is presented.
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