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      A practical guide to methods controlling false discoveries in computational biology.

      Genome Biology
      Springer Science and Business Media LLC
      ScRNA-seq, Multiple hypothesis testing, Gene set analysis, RNA-seq, False discovery rate, ChIP-seq, GWAS, Microbiome

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          Abstract

          In high-throughput studies, hundreds to millions of hypotheses are typically tested. Statistical methods that control the false discovery rate (FDR) have emerged as popular and powerful tools for error rate control. While classic FDR methods use only p values as input, more modern FDR methods have been shown to increase power by incorporating complementary information as informative covariates to prioritize, weight, and group hypotheses. However, there is currently no consensus on how the modern methods compare to one another. We investigate the accuracy, applicability, and ease of use of two classic and six modern FDR-controlling methods by performing a systematic benchmark comparison using simulation studies as well as six case studies in computational biology.

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          Most cited references38

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          Controlling the False Discovery Rate: A Practical and Powerful Approach to Multiple Testing

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            An algorithm for fast preranked gene set enrichment analysis using cumulative statistic calculation

            Gene set enrichment analysis is a widely used tool for analyzing gene expression data. However, current implementations are slow due to a large number of required samples for the analysis to have a good statistical power. In this paper we present a novel algorithm, that efficiently reuses one sample multiple times and thus speeds up the analysis. We show that it is possible to make hundreds of thousands permutations in a few minutes, which leads to very accurate p-values. This, in turn, allows applying standard FDR correction procedures, which are more accurate than the ones currently used. The method is implemented in a form of an R package and is freely available at \url{https://github.com/ctlab/fgsea}.
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              A step-by-step workflow for low-level analysis of single-cell RNA-seq data with Bioconductor

              Single-cell RNA sequencing (scRNA-seq) is widely used to profile the transcriptome of individual cells. This provides biological resolution that cannot be matched by bulk RNA sequencing, at the cost of increased technical noise and data complexity. The differences between scRNA-seq and bulk RNA-seq data mean that the analysis of the former cannot be performed by recycling bioinformatics pipelines for the latter. Rather, dedicated single-cell methods are required at various steps to exploit the cellular resolution while accounting for technical noise. This article describes a computational workflow for low-level analyses of scRNA-seq data, based primarily on software packages from the open-source Bioconductor project. It covers basic steps including quality control, data exploration and normalization, as well as more complex procedures such as cell cycle phase assignment, identification of highly variable and correlated genes, clustering into subpopulations and marker gene detection. Analyses were demonstrated on gene-level count data from several publicly available datasets involving haematopoietic stem cells, brain-derived cells, T-helper cells and mouse embryonic stem cells. This will provide a range of usage scenarios from which readers can construct their own analysis pipelines.
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                Author and article information

                Journal
                31164141
                6547503
                10.1186/s13059-019-1716-1

                ScRNA-seq,Multiple hypothesis testing,Gene set analysis,RNA-seq,False discovery rate,ChIP-seq,GWAS,Microbiome

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