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      Benchmarking algorithms for gene regulatory network inference from single-cell transcriptomic data

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          Abstract

          We present a systematic evaluation of state-of-the-art algorithms for inferring gene regulatory networks (GRNs) from single-cell transcriptional data. As the ground truth for assessing accuracy, we use synthetic networks with predictable trajectories, literature-curated Boolean models, and diverse transcriptional regulatory networks. We develop a strategy to simulate single-cell transcriptional data from synthetic and Boolean networks that avoids pitfalls of previously-used methods. Furthermore, we collect networks from multiple experimental single-cell RNA-seq datasets. We develop an evaluation framework called BEELINE. We find that the AUPRC and early precision of the algorithms are moderate. The methods are better in recovering interactions in synthetic networks than Boolean models. The algorithms with the best early precision values for Boolean models also perform well on experimental datasets. Techniques that do not require pseudotime-ordered cells are generally more accurate. Based on these results, we present recommendations to end users. BEELINE will aid the development of GRN inference algorithms.

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          Most cited references24

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          Accounting for technical noise in single-cell RNA-seq experiments.

          Single-cell RNA-seq can yield valuable insights about the variability within a population of seemingly homogeneous cells. We developed a quantitative statistical method to distinguish true biological variability from the high levels of technical noise in single-cell experiments. Our approach quantifies the statistical significance of observed cell-to-cell variability in expression strength on a gene-by-gene basis. We validate our approach using two independent data sets from Arabidopsis thaliana and Mus musculus.
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            Single cell RNA Seq reveals dynamic paracrine control of cellular variation

            High-throughput single-cell transcriptomics offers an unbiased approach for understanding the extent, basis, and function of gene expression variation between seemingly identical cells. Here, we sequence single-cell RNA-Seq libraries prepared from over 1,700 primary mouse bone marrow derived dendritic cells (DCs) spanning several experimental conditions. We find substantial variation between identically stimulated DCs, in both the fraction of cells detectably expressing a given mRNA and the transcript’s level within expressing cells. Distinct gene modules are characterized by different temporal heterogeneity profiles. In particular, a “core” module of antiviral genes is expressed very early by a few “precocious” cells, but is later activated in all cells. By stimulating cells individually in sealed microfluidic chambers, analyzing DCs from knockout mice, and modulating secretion and extracellular signaling, we show that this response is coordinated via interferon-mediated paracrine signaling. Surprisingly, preventing cell-to-cell communication also substantially reduces variability in the expression of an early-induced “peaked” inflammatory module, suggesting that paracrine signaling additionally represses part of the inflammatory program. Our study highlights the importance of cell-to-cell communication in controlling cellular heterogeneity and reveals general strategies that multicellular populations use to establish complex dynamic responses.
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              ppcor: An R Package for a Fast Calculation to Semi-partial Correlation Coefficients.

              Lack of a general matrix formula hampers implementation of the semi-partial correlation, also known as part correlation, to the higher-order coefficient. This is because the higher-order semi-partial correlation calculation using a recursive formula requires an enormous number of recursive calculations to obtain the correlation coefficients. To resolve this difficulty, we derive a general matrix formula of the semi-partial correlation for fast computation. The semi-partial correlations are then implemented on an R package ppcor along with the partial correlation. Owing to the general matrix formulas, users can readily calculate the coefficients of both partial and semi-partial correlations without computational burden. The package ppcor further provides users with the level of the statistical significance with its test statistic.
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                Author and article information

                Journal
                101215604
                32338
                Nat Methods
                Nat. Methods
                Nature methods
                1548-7091
                1548-7105
                22 November 2019
                06 January 2020
                February 2020
                06 July 2020
                : 17
                : 2
                : 147-154
                Affiliations
                [1 ]Department of Computer Science, Virginia Tech, Blacksburg, USA 24060
                [2 ]Genetics, Bioinformatics, and Computational Biology Ph.D. Program, Virginia Tech, Blacksburg, USA 24060
                Author notes

                Author contributions

                AP and TMM conceived and designed the analysis and selected the GRN algorithms. AP implemented BEELINE and led the analysis. APJ, AP, and TMM developed BoolODE and APJ implemented it. AP and APJ created and processed datasets. AP, APJ, JNL, and AB contributed evaluation strategies. All authors analyzed the results. AP, APJ, and TMM wrote the paper. TMM supervised the project.

                [* ]Correspondence: T. M. Murali ( murali@ 123456cs.vt.edu )
                Article
                NIHMS1544277
                10.1038/s41592-019-0690-6
                7098173
                31907445
                ac1d858b-fa02-4536-8a1d-46298f4bf8fd

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