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      Genomic Prediction Including SNP-Specific Variance Predictors

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          Abstract

          The increasing amount of available biological information on the markers can be used to inform the models applied for genomic selection to improve predictions. The objective of this study was to propose a general model for genomic selection using a link function approach within the hierarchical generalized linear model framework (hglm) that can include external information on the markers. These models can be fitted using the well-established hglm package in R. We also present an R package (CodataGS) to fit these models, which is significantly faster than the hglm package. Simulated data were used to validate the proposed model. We tested categorical, continuous and combination models where the external information on the markers was related to 1) the location of the QTL on the genome with varying degree of uncertainty, 2) the relationship of the markers with the QTL calculated as the LD between them, and 3) a combination of both. The proposed models showed improved accuracies from 3.8% up to 23.2% compared to the SNP-BLUP method in a simulated population derived from a base population with 100 individuals. Moreover, the proposed categorical model was tested on a dairy cattle dataset for two traits (Milk Yield and Fat Percentage). These results also showed improved accuracy compared to SNP-BLUP, especially for the Fat% trait. The performance of the proposed models depended on the genetic architecture of the trait, as traits that deviate from the infinitesimal model benefited more from the external information. Also, the gain in accuracy depended on the degree of uncertainty of the external information provided to the model. The usefulness of these type of models is expected to increase with time as more accurate information on the markers becomes available.

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          Most cited references44

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          Introduction to Quantitative Genetics

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            Transcriptional regulatory networks in Saccharomyces cerevisiae.

            We have determined how most of the transcriptional regulators encoded in the eukaryote Saccharomyces cerevisiae associate with genes across the genome in living cells. Just as maps of metabolic networks describe the potential pathways that may be used by a cell to accomplish metabolic processes, this network of regulator-gene interactions describes potential pathways yeast cells can use to regulate global gene expression programs. We use this information to identify network motifs, the simplest units of network architecture, and demonstrate that an automated process can use motifs to assemble a transcriptional regulatory network structure. Our results reveal that eukaryotic cellular functions are highly connected through networks of transcriptional regulators that regulate other transcriptional regulators.
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              Chapter 11: Genome-Wide Association Studies

              Genome-wide association studies (GWAS) have evolved over the last ten years into a powerful tool for investigating the genetic architecture of human disease. In this work, we review the key concepts underlying GWAS, including the architecture of common diseases, the structure of common human genetic variation, technologies for capturing genetic information, study designs, and the statistical methods used for data analysis. We also look forward to the future beyond GWAS.
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                Author and article information

                Journal
                G3 (Bethesda)
                Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes, Genomes, Genetics
                G3: Genes|Genomes|Genetics
                Genetics Society of America
                2160-1836
                29 August 2019
                October 2019
                : 9
                : 10
                : 3333-3343
                Affiliations
                [* ]Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Sweden, 75007,
                []Department of Mathematical Sciences, Norwegian University of Science and Technology, Norway, 7491, and
                []School of Technology and Business Studies, Dalarna University, Sweden, 79188
                Author notes
                [1 ]Corresponding author: Department of Animal Breeding and Genetics, Swedish University of Agricultural Sciences, Ulls väg 26, Box 7023, 75007 Uppsala, Sweden. E-mail: elena.flavia.mouresan@ 123456slu.se
                Author information
                http://orcid.org/0000-0002-1335-7610
                http://orcid.org/0000-0002-2062-3235
                http://orcid.org/0000-0002-1057-5401
                Article
                GGG_400381
                10.1534/g3.119.400381
                6778789
                31467030
                2c74c9f3-0764-466b-94bd-5d8568de5502
                Copyright © 2019 Mouresan et al.

                This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 30 May 2019
                : 09 August 2019
                Page count
                Figures: 4, Tables: 3, Equations: 5, References: 61, Pages: 11
                Categories
                Genomic Prediction

                Genetics
                blup,hglm,codatags,external information,genomic prediction,genpred,shared data resources
                Genetics
                blup, hglm, codatags, external information, genomic prediction, genpred, shared data resources

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