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      Genome sequence of the Asian Tiger mosquito, Aedes albopictus, reveals insights into its biology, genetics, and evolution.

      1 , 2 , 3 , 2 , 3 , 3 , 2 , 4 ,   5 , 6 , 7 , 7 , 2 , 3 , 2 , 3 , 2 , 3 , 2 , 8 , 9 , 10 , 11 , 11 , 12 , 13 , 13 , 14 , 15 , 11 , 16 , 17
      Proceedings of the National Academy of Sciences of the United States of America
      diapause, flavivirus, insecticide resistance, mosquito genome, transposons

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          Abstract

          The Asian tiger mosquito, Aedes albopictus, is a highly successful invasive species that transmits a number of human viral diseases, including dengue and Chikungunya fevers. This species has a large genome with significant population-based size variation. The complete genome sequence was determined for the Foshan strain, an established laboratory colony derived from wild mosquitoes from southeastern China, a region within the historical range of the origin of the species. The genome comprises 1,967 Mb, the largest mosquito genome sequenced to date, and its size results principally from an abundance of repetitive DNA classes. In addition, expansions of the numbers of members in gene families involved in insecticide-resistance mechanisms, diapause, sex determination, immunity, and olfaction also contribute to the larger size. Portions of integrated flavivirus-like genomes support a shared evolutionary history of association of these viruses with their vector. The large genome repertory may contribute to the adaptability and success of Ae. albopictus as an invasive species.

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          Most cited references62

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          Identification of novel transcripts in annotated genomes using RNA-Seq.

          We describe a new 'reference annotation based transcript assembly' problem for RNA-Seq data that involves assembling novel transcripts in the context of an existing annotation. This problem arises in the analysis of expression in model organisms, where it is desirable to leverage existing annotations for discovering novel transcripts. We present an algorithm for reference annotation-based transcript assembly and show how it can be used to rapidly investigate novel transcripts revealed by RNA-Seq in comparison with a reference annotation. The methods described in this article are implemented in the Cufflinks suite of software for RNA-Seq, freely available from http://bio.math.berkeley.edu/cufflinks. The software is released under the BOOST license. cole@broadinstitute.org; lpachter@math.berkeley.edu Supplementary data are available at Bioinformatics online.
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            Ab initio gene finding in Drosophila genomic DNA.

            Ab initio gene identification in the genomic sequence of Drosophila melanogaster was obtained using (human gene predictor) and Fgenesh programs that have organism-specific parameters for human, Drosophila, plants, yeast, and nematode. We did not use information about cDNA/EST in most predictions to model a real situation for finding new genes because information about complete cDNA is often absent or based on very small partial fragments. We investigated the accuracy of gene prediction on different levels and designed several schemes to predict an unambiguous set of genes (annotation CGG1), a set of reliable exons (annotation CGG2), and the most complete set of exons (annotation CGG3). For 49 genes, protein products of which have clear homologs in protein databases, predictions were recomputed by Fgenesh+ program. The first annotation serves as the optimal computational description of new sequence to be presented in a database. Reliable exons from the second annotation serve as good candidates for selecting the PCR primers for experimental work for gene structure verification. Our results shows that we can identify approximately 90% of coding nucleotides with 20% false positives. At the exon level we accurately predicted 65% of exons and 89% including overlapping exons with 49% false positives. Optimizing accuracy of prediction, we designed a gene identification scheme using Fgenesh, which provided sensitivity (Sn) = 98% and specificity (Sp) = 86% at the base level, Sn = 81% (97% including overlapping exons) and Sp = 58% at the exon level and Sn = 72% and Sp = 39% at the gene level (estimating sensitivity on std1 set and specificity on std3 set). In general, these results showed that computational gene prediction can be a reliable tool for annotating new genomic sequences, giving accurate information on 90% of coding sequences with 14% false positives. However, exact gene prediction (especially at the gene level) needs additional improvement using gene prediction algorithms. The program was also tested for predicting genes of human Chromosome 22 (the last variant of Fgenesh can analyze the whole chromosome sequence). This analysis has demonstrated that the 88% of manually annotated exons in Chromosome 22 were among the ab initio predicted exons. The suite of gene identification programs is available through the WWW server of Computational Genomics Group at http://genomic.sanger.ac.uk/gf. html.
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              Evolutionary dynamics of immune-related genes and pathways in disease-vector mosquitoes.

              Mosquitoes are vectors of parasitic and viral diseases of immense importance for public health. The acquisition of the genome sequence of the yellow fever and Dengue vector, Aedes aegypti (Aa), has enabled a comparative phylogenomic analysis of the insect immune repertoire: in Aa, the malaria vector Anopheles gambiae (Ag), and the fruit fly Drosophila melanogaster (Dm). Analysis of immune signaling pathways and response modules reveals both conservative and rapidly evolving features associated with different functional gene categories and particular aspects of immune reactions. These dynamics reflect in part continuous readjustment between accommodation and rejection of pathogens and suggest how innate immunity may have evolved.
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                Author and article information

                Journal
                Proc. Natl. Acad. Sci. U.S.A.
                Proceedings of the National Academy of Sciences of the United States of America
                1091-6490
                0027-8424
                Nov 3 2015
                : 112
                : 44
                Affiliations
                [1 ] Department of Pathogen Biology, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China; 18664867266@qq.com fangxd@genomics.cn aajames@uci.edu.
                [2 ] Beijing Genomics Institute-Shenzhen, Shenzhen 518083, China;
                [3 ] Department of Pathogen Biology, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China;
                [4 ] Program in Public Health, University of California, Irvine, CA 92697; Department of Biology and Biotechnology, University of Pavia, 27100 Pavia, Italy;
                [5 ] Laboratory of Agrozoology, Department of Crop Protection, Faculty of Bioscience Engineering, Ghent University, B-9000 Ghent, Belgium;
                [6 ] Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, 73100 Heraklion, Greece; Faculty of Crop Science, Pesticide Science Lab, Agricultural University of Athens, 11855 Athens, Greece;
                [7 ] Department of Biology, Georgetown University, Washington, DC 20057;
                [8 ] Department of Biology, University of Crete, Heraklion, GR-74100, Crete, Greece;
                [9 ] Institute of Molecular Biology and Biotechnology, Foundation for Research and Technology-Hellas, 73100 Heraklion, Greece;
                [10 ] Department of Biology and Biotechnology, University of Pavia, 27100 Pavia, Italy; Institute for Biodiversity and Ecosystem Dynamics, University of Amsterdam, 1090 GE Amsterdam, The Netherlands;
                [11 ] Interdisciplinary PhD Program in Genetics, Bioinformatics, and Computational Biology, Virginia Tech University, Blacksburg, VA 24061; Department of Biochemistry, Fralin Life Science Institute, Virginia Tech University, Blacksburg, VA 24061;
                [12 ] Cellular and Molecular Physiology, Edward Via College of Osteopathic Medicine, Blacksburg, VA 24060;
                [13 ] Department of Biology, Colorado State University, Fort Collins, CO 80523;
                [14 ] Department of Genetic Medicine and Development, University of Geneva Medical School, 1211 Geneva, Switzerland; Swiss Institute of Bioinformatics, 1211 Geneva, Switzerland; Computer Science and Artificial Intelligence Laboratory, Massachusetts Institute of Technology, Cambridge, MA 02139; The Broad Institute of MIT and Harvard, Cambridge, MA 02142;
                [15 ] Department of Pathogen Biology, School of Public Health and Tropical Medicine, Southern Medical University, Guangzhou 510515, China; Program in Public Health, University of California, Irvine, CA 92697;
                [16 ] Beijing Genomics Institute-Shenzhen, Shenzhen 518083, China; 18664867266@qq.com fangxd@genomics.cn aajames@uci.edu.
                [17 ] Departments of Microbiology & Molecular Genetics and Molecular Biology & Biochemistry, University of California, Irvine, CA 92697 18664867266@qq.com fangxd@genomics.cn aajames@uci.edu.
                Article
                1516410112
                10.1073/pnas.1516410112
                26483478
                d49b865a-3c5d-4bf9-91a0-667bdf61d6d0
                History

                diapause,flavivirus,insecticide resistance,mosquito genome,transposons

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