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      Edge and modular significance assessment in individual-specific networks

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          Abstract

          Individual-specific networks, defined as networks of nodes and connecting edges that are specific to an individual, are promising tools for precision medicine. When such networks are biological, interpretation of functional modules at an individual level becomes possible. An under-investigated problem is relevance or ”significance” assessment of each individual-specific network. This paper proposes novel edge and module significance assessment procedures for weighted and unweighted individual-specific networks. Specifically, we propose a modular Cook’s distance using a method that involves iterative modeling of one edge versus all the others within a module. Two procedures assessing changes between using all individuals and using all individuals but leaving one individual out (LOO) are proposed as well ( LOO-ISN, MultiLOO-ISN), relying on empirically derived edges. We compare our proposals to competitors, including adaptions of OPTICS, kNN, and Spoutlier methods, by an extensive simulation study, templated on real-life scenarios for gene co-expression and microbial interaction networks. Results show the advantages of performing modular versus edge-wise significance assessments for individual-specific networks. Furthermore, modular Cook’s distance is among the top performers across all considered simulation settings. Finally, the identification of outlying individuals regarding their individual-specific networks, is meaningful for precision medicine purposes, as confirmed by network analysis of microbiome abundance profiles.

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          Differential expression analysis for sequence count data

          High-throughput sequencing assays such as RNA-Seq, ChIP-Seq or barcode counting provide quantitative readouts in the form of count data. To infer differential signal in such data correctly and with good statistical power, estimation of data variability throughout the dynamic range and a suitable error model are required. We propose a method based on the negative binomial distribution, with variance and mean linked by local regression and present an implementation, DESeq, as an R/Bioconductor package.
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            Delivery mode shapes the acquisition and structure of the initial microbiota across multiple body habitats in newborns.

            Upon delivery, the neonate is exposed for the first time to a wide array of microbes from a variety of sources, including maternal bacteria. Although prior studies have suggested that delivery mode shapes the microbiota's establishment and, subsequently, its role in child health, most researchers have focused on specific bacterial taxa or on a single body habitat, the gut. Thus, the initiation stage of human microbiome development remains obscure. The goal of the present study was to obtain a community-wide perspective on the influence of delivery mode and body habitat on the neonate's first microbiota. We used multiplexed 16S rRNA gene pyrosequencing to characterize bacterial communities from mothers and their newborn babies, four born vaginally and six born via Cesarean section. Mothers' skin, oral mucosa, and vagina were sampled 1 h before delivery, and neonates' skin, oral mucosa, and nasopharyngeal aspirate were sampled <5 min, and meconium <24 h, after delivery. We found that in direct contrast to the highly differentiated communities of their mothers, neonates harbored bacterial communities that were undifferentiated across multiple body habitats, regardless of delivery mode. Our results also show that vaginally delivered infants acquired bacterial communities resembling their own mother's vaginal microbiota, dominated by Lactobacillus, Prevotella, or Sneathia spp., and C-section infants harbored bacterial communities similar to those found on the skin surface, dominated by Staphylococcus, Corynebacterium, and Propionibacterium spp. These findings establish an important baseline for studies tracking the human microbiome's successional development in different body habitats following different delivery modes, and their associated effects on infant health.
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              Network medicine: a network-based approach to human disease.

              Given the functional interdependencies between the molecular components in a human cell, a disease is rarely a consequence of an abnormality in a single gene, but reflects the perturbations of the complex intracellular and intercellular network that links tissue and organ systems. The emerging tools of network medicine offer a platform to explore systematically not only the molecular complexity of a particular disease, leading to the identification of disease modules and pathways, but also the molecular relationships among apparently distinct (patho)phenotypes. Advances in this direction are essential for identifying new disease genes, for uncovering the biological significance of disease-associated mutations identified by genome-wide association studies and full-genome sequencing, and for identifying drug targets and biomarkers for complex diseases.
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                Author and article information

                Contributors
                federico.melograna@kuleuven.be
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                15 May 2023
                15 May 2023
                2023
                : 13
                : 7868
                Affiliations
                [1 ]GRID grid.5596.f, ISNI 0000 0001 0668 7884, BIO3 - Laboratory for Systems Medicine, Department of Human Genetics, , KU Leuven, ; Leuven, Belgium
                [2 ]GRID grid.412966.e, ISNI 0000 0004 0480 1382, School of Nutrition and Translational Research in Metabolism (NUTRIM), Department of Medical Microbiology Infectious Diseases and Infection Prevention, , Maastricht University Medical Center+, ; Maastricht, The Netherlands
                [3 ]GRID grid.1957.a, ISNI 0000 0001 0728 696X, Institute of Medical Microbiology, RWTH University Hospital Aachen, , RWTH University, ; Aachen, Germany
                [4 ]GRID grid.5012.6, ISNI 0000 0001 0481 6099, Department of Epidemiology, Care and Public Health Research Institute (CAPHRI), , Maastricht University, ; Maastricht, The Netherlands
                [5 ]GRID grid.5012.6, ISNI 0000 0001 0481 6099, Care and Public Health Research Institute (CAPHRI), , Maastricht University, ; Maastricht, The Netherlands
                [6 ]GRID grid.7563.7, ISNI 0000 0001 2174 1754, Department of Informatics, Systems and Communication, , University of Milano-Bicocca, ; 20126 Milan, Italy
                [7 ]GRID grid.4861.b, ISNI 0000 0001 0805 7253, BIO3 - Laboratory for Systems Genetics, GIGA-R Medical Genomics, , University of Liège, ; Liège, Belgium
                Article
                34759
                10.1038/s41598-023-34759-8
                10185658
                37188794
                74db648b-d70d-4dbe-bca0-5d8dbec8ed63
                © The Author(s) 2023

                Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 19 September 2022
                : 7 May 2023
                Funding
                Funded by: European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie
                Award ID: 860895
                Funded by: European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreements
                Award ID: 813533
                Award Recipient :
                Categories
                Article
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                © Springer Nature Limited 2023

                Uncategorized
                computational biology and bioinformatics,machine learning,network topology,microbial communities,microbiome

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