37
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Deep Generative Modeling for Single-cell Transcriptomics

      research-article

      Read this article at

      ScienceOpenPublisherPMC
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Transcriptome measurements of individual cells reflect unexplored biological diversity, but are also affected by technical noise and bias. This raises the need to model and account for the resulting uncertainty in any downstream analysis. Here, we introduce Single-cell Variational Inference (scVI), a scalable framework for probabilistic representation and analysis of gene expression in single cells. scVI uses stochastic optimization and deep neural networks to aggregate information across similar cells and genes and approximate the distributions that underlie the observed expression values, while accounting for batch effects and limited sensitivity. We utilize scVI for a range of fundamental analysis tasks – including batch correction, visualization, clustering and differential expression – and demonstrate its accuracy and scalability in comparison to the state-of-the-art in each task. scVI is publicly available and can be readily used as a principled and inclusive solution for analyzing single-cell transcriptomes.

          Related collections

          Most cited references14

          • Record: found
          • Abstract: found
          • Article: not found

          Systems Biology of Seasonal Influenza Vaccination in Humans

          We used a systems biological approach to study innate and adaptive responses to influenza vaccination in humans, during 3 consecutive influenza seasons. Healthy adults were vaccinated with inactivated (TIV) or live attenuated (LAIV) influenza vaccines. TIV induced greater antibody titers and enhanced numbers of plasmablasts than LAIV. In TIV vaccinees, early molecular signatures correlated with, and accurately predicted, later antibody titers in two independent trials. Interestingly, the expression of Calcium/calmodulin-dependent kinase IV (CamkIV) at day 3 was inversely correlated with later antibody titers. Vaccination of CamkIV −/− mice with TIV induced enhanced antigen-specific antibody titers, demonstrating an unappreciated role for CaMKIV in the regulation of antibody responses. Thus systems approaches can predict immunogenicity, and reveal new mechanistic insights about vaccines.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Single-Cell Genomics Unveils Critical Regulators of Th17 Cell Pathogenicity.

            Extensive cellular heterogeneity exists within specific immune-cell subtypes classified as a single lineage, but its molecular underpinnings are rarely characterized at a genomic scale. Here, we use single-cell RNA-seq to investigate the molecular mechanisms governing heterogeneity and pathogenicity of Th17 cells isolated from the central nervous system (CNS) and lymph nodes (LN) at the peak of autoimmune encephalomyelitis (EAE) or differentiated in vitro under either pathogenic or non-pathogenic polarization conditions. Computational analysis relates a spectrum of cellular states in vivo to in-vitro-differentiated Th17 cells and unveils genes governing pathogenicity and disease susceptibility. Using knockout mice, we validate four new genes: Gpr65, Plzp, Toso, and Cd5l (in a companion paper). Cellular heterogeneity thus informs Th17 function in autoimmunity and can identify targets for selective suppression of pathogenic Th17 cells while potentially sparing non-pathogenic tissue-protective ones.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: found
              Is Open Access

              A general and flexible method for signal extraction from single-cell RNA-seq data

              Single-cell RNA-sequencing (scRNA-seq) is a powerful high-throughput technique that enables researchers to measure genome-wide transcription levels at the resolution of single cells. Because of the low amount of RNA present in a single cell, some genes may fail to be detected even though they are expressed; these genes are usually referred to as dropouts. Here, we present a general and flexible zero-inflated negative binomial model (ZINB-WaVE), which leads to low-dimensional representations of the data that account for zero inflation (dropouts), over-dispersion, and the count nature of the data. We demonstrate, with simulated and real data, that the model and its associated estimation procedure are able to give a more stable and accurate low-dimensional representation of the data than principal component analysis (PCA) and zero-inflated factor analysis (ZIFA), without the need for a preliminary normalization step.
                Bookmark

                Author and article information

                Journal
                101215604
                32338
                Nat Methods
                Nat. Methods
                Nature methods
                1548-7091
                1548-7105
                14 November 2018
                30 November 2018
                December 2018
                30 May 2019
                : 15
                : 12
                : 1053-1058
                Affiliations
                [1 ]Department of Electrical Engineering and Computer Sciences, University of California, Berkeley
                [2 ]Department of Physics, University of California, Berkeley
                [3 ]Department of Statistics, University of California, Berkeley
                [5 ]Ragon Institute of MGH, MIT and Harvard
                [6 ]Chan-Zuckerberg Biohub Investigator
                Author notes

                Author contributions

                RL, JR, and NY conceived the statistical model. RL developed the software. RL and MBC applied the software to real data analysis. RL, JR, NY, and MIJ wrote the manuscript. NY and MIJ supervised the work.

                Correspondence should be addressed to N.Y ( niryosef@ 123456berkeley.edu )
                Article
                NIHMS1510930
                10.1038/s41592-018-0229-2
                6289068
                30504886
                0866bffa-32ea-41b4-9889-ce0844b4e7c0

                Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms

                History
                Categories
                Article

                Life sciences
                Life sciences

                Comments

                Comment on this article