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      NanoStringDiff: a novel statistical method for differential expression analysis based on NanoString nCounter data

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          Abstract

          The advanced medium-throughput NanoString nCounter technology has been increasingly used for mRNA or miRNA differential expression (DE) studies due to its advantages including direct measurement of molecule expression levels without amplification, digital readout and superior applicability to formalin fixed paraffin embedded samples. However, the analysis of nCounter data is hampered because most methods developed are based on t-tests, which do not fit the count data generated by the NanoString nCounter system. Furthermore, data normalization procedures of current methods are either not suitable for counts or not specific for NanoString nCounter data. We develop a novel DE detection method based on NanoString nCounter data. The method, named NanoStringDiff, considers a generalized linear model of the negative binomial family to characterize count data and allows for multifactor design. Data normalization is incorporated in the model framework through data normalization parameters, which are estimated from positive controls, negative controls and housekeeping genes embedded in the nCounter system. We propose an empirical Bayes shrinkage approach to estimate the dispersion parameter in the model and a likelihood ratio test to identify differentially expressed genes. Simulations and real data analysis demonstrate that the proposed method performs better than existing methods.

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

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            Direct multiplexed measurement of gene expression with color-coded probe pairs.

            We describe a technology, the NanoString nCounter gene expression system, which captures and counts individual mRNA transcripts. Advantages over existing platforms include direct measurement of mRNA expression levels without enzymatic reactions or bias, sensitivity coupled with high multiplex capability, and digital readout. Experiments performed on 509 human genes yielded a replicate correlation coefficient of 0.999, a detection limit between 0.1 fM and 0.5 fM, and a linear dynamic range of over 500-fold. Comparison of the NanoString nCounter gene expression system with microarrays and TaqMan PCR demonstrated that the nCounter system is more sensitive than microarrays and similar in sensitivity to real-time PCR. Finally, a comparison of transcript levels for 21 genes across seven samples measured by the nCounter system and SYBR Green real-time PCR demonstrated similar patterns of gene expression at all transcript levels.
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              Small-sample estimation of negative binomial dispersion, with applications to SAGE data.

              We derive a quantile-adjusted conditional maximum likelihood estimator for the dispersion parameter of the negative binomial distribution and compare its performance, in terms of bias, to various other methods. Our estimation scheme outperforms all other methods in very small samples, typical of those from serial analysis of gene expression studies, the motivating data for this study. The impact of dispersion estimation on hypothesis testing is studied. We derive an "exact" test that outperforms the standard approximate asymptotic tests.
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                Author and article information

                Journal
                Nucleic Acids Res
                Nucleic Acids Res
                nar
                nar
                Nucleic Acids Research
                Oxford University Press
                0305-1048
                1362-4962
                16 November 2016
                28 July 2016
                28 July 2016
                : 44
                : 20
                : e151
                Affiliations
                [1 ]Department of Statistics, University of Kentucky, Lexington, KY 40536, USA
                [2 ]Departments of Pathology and Neurosurgery, Northwestern University, Chicago, IL 60611, USA
                [3 ]Department of Biostatistics and Bioinformatics, Emory University, Atlanta, GA 30322, USA
                [4 ]Department of Pathology and Laboratory Medicine, University of Kentucky, Lexington, KY 40536 USA
                [5 ]Paul Laurence Dunbar High School, Lexington, KY 40513, USA
                [6 ]Biostatistics and Bioinformatics Shared Resource Facility, Markey Cancer Center, University of Kentucky, Lexington, KY 40536, USA
                [7 ]Department of Biostatistics, University of Kentucky, Lexington, KY 40536, USA
                Author notes
                [* ]To whom correspondence should be addressed. Tel: +1 859 323 2045; Fax: +1 859 323 2074; Email: chi.wang@ 123456uky.edu
                Article
                10.1093/nar/gkw677
                5175344
                27471031
                b160ecfc-975f-454d-9740-c375f0da0669
                © The Author(s) 2016. Published by Oxford University Press on behalf of Nucleic Acids Research.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@ 123456oup.com

                History
                : 18 July 2016
                : 10 July 2016
                : 17 February 2016
                Page count
                Pages: 9
                Categories
                7
                24
                Methods Online
                Custom metadata
                16 November 2016

                Genetics
                Genetics

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