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      Predicting susceptibility to tuberculosis based on gene expression profiling in dendritic cells

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          Abstract

          Tuberculosis (TB) is a deadly infectious disease, which kills millions of people every year. The causative pathogen, Mycobacterium tuberculosis (MTB), is estimated to have infected up to a third of the world’s population; however, only approximately 10% of infected healthy individuals progress to active TB. Despite evidence for heritability, it is not currently possible to predict who may develop TB. To explore approaches to classify susceptibility to TB, we infected with MTB dendritic cells (DCs) from putatively resistant individuals diagnosed with latent TB, and from susceptible individuals that had recovered from active TB. We measured gene expression levels in infected and non-infected cells and found hundreds of differentially expressed genes between susceptible and resistant individuals in the non-infected cells. We further found that genetic polymorphisms nearby the differentially expressed genes between susceptible and resistant individuals are more likely to be associated with TB susceptibility in published GWAS data. Lastly, we trained a classifier based on the gene expression levels in the non-infected cells, and demonstrated reasonable performance on our data and an independent data set. Overall, our promising results from this small study suggest that training a classifier on a larger cohort may enable us to accurately predict TB susceptibility.

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          Most cited references36

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          featureCounts: An efficient general-purpose program for assigning sequence reads to genomic features

          , , (2013)
          Next-generation sequencing technologies generate millions of short sequence reads, which are usually aligned to a reference genome. In many applications, the key information required for downstream analysis is the number of reads mapping to each genomic feature, for example to each exon or each gene. The process of counting reads is called read summarization. Read summarization is required for a great variety of genomic analyses but has so far received relatively little attention in the literature. We present featureCounts, a read summarization program suitable for counting reads generated from either RNA or genomic DNA sequencing experiments. featureCounts implements highly efficient chromosome hashing and feature blocking techniques. It is considerably faster than existing methods (by an order of magnitude for gene-level summarization) and requires far less computer memory. It works with either single or paired-end reads and provides a wide range of options appropriate for different sequencing applications. featureCounts is available under GNU General Public License as part of the Subread (http://subread.sourceforge.net) or Rsubread (http://www.bioconductor.org) software packages.
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            Latent enhancers activated by stimulation in differentiated cells.

            According to current models, once the cell has reached terminal differentiation, the enhancer repertoire is completely established and maintained by cooperatively acting lineage-specific transcription factors (TFs). TFs activated by extracellular stimuli operate within this predetermined repertoire, landing close to where master regulators are constitutively bound. Here, we describe latent enhancers, defined as regions of the genome that in terminally differentiated cells are unbound by TFs and lack the histone marks characteristic of enhancers but acquire these features in response to stimulation. Macrophage stimulation caused sequential binding of stimulus-activated and lineage-determining TFs to these regions, enabling deposition of enhancer marks. Once unveiled, many of these enhancers did not return to a latent state when stimulation ceased; instead, they persisted and mediated a faster and stronger response upon restimulation. We suggest that stimulus-specific expansion of the cis-regulatory repertoire provides an epigenomic memory of the exposure to environmental agents. Copyright © 2013 Elsevier Inc. All rights reserved.
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              Why weight? Modelling sample and observational level variability improves power in RNA-seq analyses

              Variations in sample quality are frequently encountered in small RNA-sequencing experiments, and pose a major challenge in a differential expression analysis. Removal of high variation samples reduces noise, but at a cost of reducing power, thus limiting our ability to detect biologically meaningful changes. Similarly, retaining these samples in the analysis may not reveal any statistically significant changes due to the higher noise level. A compromise is to use all available data, but to down-weight the observations from more variable samples. We describe a statistical approach that facilitates this by modelling heterogeneity at both the sample and observational levels as part of the differential expression analysis. At the sample level this is achieved by fitting a log-linear variance model that includes common sample-specific or group-specific parameters that are shared between genes. The estimated sample variance factors are then converted to weights and combined with observational level weights obtained from the mean–variance relationship of the log-counts-per-million using ‘voom’. A comprehensive analysis involving both simulations and experimental RNA-sequencing data demonstrates that this strategy leads to a universally more powerful analysis and fewer false discoveries when compared to conventional approaches. This methodology has wide application and is implemented in the open-source ‘limma’ package.
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                Author and article information

                Contributors
                tailleux@pasteur.fr
                luis.barreiro@umontreal.ca
                gilad@uchicago.edu
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                18 July 2017
                18 July 2017
                2017
                : 7
                : 5702
                Affiliations
                [1 ]ISNI 0000 0004 1936 7822, GRID grid.170205.1, Department of Human Genetics, , University of Chicago, ; Chicago, Illinois USA
                [2 ]ISNI 0000 0004 1936 7822, GRID grid.170205.1, Committee on Genetics, Genomics, and Systems Biology, , University of Chicago, ; Chicago, Illinois USA
                [3 ]ISNI 0000 0001 2353 6535, GRID grid.428999.7, Integrated Mycobacterial Pathogenomics, , Institut Pasteur, ; Paris, France
                [4 ]Centre de Lutte Antituberculeuse de Paris, DASES Mairie de Paris, 75013 Paris, France
                [5 ]ISNI 0000 0004 0472 0160, GRID grid.411149.8, Service de pneumologie et oncologie thoracique, , CHU Côte de Nacre, ; 14033 Caen, France
                [6 ]Maladies Infectieuses, AP-HP, Hôpital Universitaire Raymond-Poincaré, Garches, 92380 France
                [7 ]ISNI 0000 0001 2353 6535, GRID grid.428999.7, Clinical Investigation & Access Biological Resources (ICAReB), , Institut Pasteur, ; Paris, France
                [8 ]ISNI 0000 0001 2353 6535, GRID grid.428999.7, Clinical Core, , Centre for Translational Science, Institut Pasteur, ; Paris, France
                [9 ]ISNI 0000 0001 2323 0229, GRID grid.12832.3a, INSERM, U1173, UFR Simone Veil, , Université de Versailles Saint Quentin, ; Saint Quentin en Yvelines, France
                [10 ]APHP, Groupe Hospitalo-Universitaire Paris Île-de-France Ouest, Garches et Boulogne-Billancourt, France
                [11 ]ISNI 0000 0001 2173 6322, GRID grid.411418.9, Department of Genetics, , CHU Sainte-Justine Research Center, ; Montreal, Québec Canada
                [12 ]ISNI 0000 0001 2292 3357, GRID grid.14848.31, Department of Pediatrics, , University of Montreal, ; Montreal, Québec Canada
                [13 ]ISNI 0000 0004 1936 7822, GRID grid.170205.1, Department of Medicine, , University of Chicago, ; Chicago, Illinois USA
                Author information
                http://orcid.org/0000-0003-2634-9879
                http://orcid.org/0000-0003-2347-6418
                http://orcid.org/0000-0003-2587-3863
                Article
                5878
                10.1038/s41598-017-05878-w
                5516010
                28720766
                69401add-59eb-4ef1-9a5d-dfdf918bb735
                © The Author(s) 2017

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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                : 13 February 2017
                : 5 June 2017
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