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      A haplotype-resolved reference genome of a long-distance migratory bat, Pipistrellus nathusii (Keyserling & Blasius, 1839)

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          Abstract

          We present a complete, chromosome-scale reference genome for the long-distance migratory bat Pipistrellus nathusii. The genome encompasses both haplotypic sets of autosomes and the separation of both sex chromosomes by utilizing highly accurate long-reads and preserving long-range phasing information through the use of three-dimensional chromatin conformation capture sequencing (Hi-C). This genome, accompanied by a comprehensive protein-coding sequence annotation, provides a valuable genomic resource for future investigations into the genomic bases of long-distance migratory flight in bats as well as uncovering the genetic architecture, population structure and evolutionary history of Pipistrellus nathusii. The reference-quality genome presented here gives a fundamental resource to further our understanding of bat genetics and evolution, adding to the growing number of high-quality genetic resources in this field. Here, we demonstrate its use in the phylogenetic reconstruction of the order Chiroptera, and in particular, we present the resources to allow detailed investigations into the genetic drivers and adaptations related to long-distance migration.

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          MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability

          We report a major update of the MAFFT multiple sequence alignment program. This version has several new features, including options for adding unaligned sequences into an existing alignment, adjustment of direction in nucleotide alignment, constrained alignment and parallel processing, which were implemented after the previous major update. This report shows actual examples to explain how these features work, alone and in combination. Some examples incorrectly aligned by MAFFT are also shown to clarify its limitations. We discuss how to avoid misalignments, and our ongoing efforts to overcome such limitations.
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            Cutadapt removes adapter sequences from high-throughput sequencing reads

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              Graph-based genome alignment and genotyping with HISAT2 and HISAT-genotype

              Rapid advances in next-generation sequencing technologies have dramatically changed our ability to perform genome-scale analyses. The human reference genome used for most genomic analyses represents only a small number of individuals, limiting its usefulness for genotyping. We designed a novel method, HISAT2, for representing and searching an expanded model of the human reference genome, in which a large catalogue of known genomic variants and haplotypes is incorporated into the data structure used for searching and alignment. This strategy for representing a population of genomes, along with a fast and memory-efficient search algorithm, enables more detailed and accurate variant analyses than previous methods. We demonstrate two initial applications of HISAT2: HLA typing, a critical need in human organ transplantation, and DNA fingerprinting, widely used in forensics. These applications are part of HISAT-genotype, with performance not only surpassing earlier computational methods, but matching or exceeding the accuracy of laboratory-based assays.
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                Author and article information

                Contributors
                Journal
                DNA Res
                DNA Res
                dnares
                DNA Research: An International Journal for Rapid Publication of Reports on Genes and Genomes
                Oxford University Press (UK )
                1340-2838
                1756-1663
                August 2024
                07 June 2024
                07 June 2024
                : 31
                : 4
                : dsae018
                Affiliations
                Berlin Center for Genomics in Biodiversity Research (BeGenDiv) , Berlin, Germany
                Evolutionary Genetics Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                Berlin Center for Genomics in Biodiversity Research (BeGenDiv) , Berlin, Germany
                Evolutionary Genetics Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                Evolutionary Ecology Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                School of Biosciences, University of Melbourne , Parkville, 3010 Victoria, Australia
                LOEWE Centre for Translational Biodiversity Genomics , Senckenberganlage 25, 60325 Frankfurt, Germany
                Senckenberg Research Institute , Senckenberganlage 25, 60325 Frankfurt, Germany
                Institute of Cell Biology and Neuroscience, Faculty of Biosciences, Goethe University Frankfurt , Max-von-Laue-Str. 9, 60438 Frankfurt, Germany
                Sequencing and Genotyping, Max Planck Institute of Molecular Cell Biology and Genetics , Pfotenhauerstraße 108, 01307 Dresden, Germany
                Sequencing and Genotyping, Max Planck Institute of Molecular Cell Biology and Genetics , Pfotenhauerstraße 108, 01307 Dresden, Germany
                Evolutionary Ecology Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                Evolutionary Genetics Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                Institute for Biochemistry and Biology, University of Potsdam , 14476 Potsdam, Germany
                Berlin Center for Genomics in Biodiversity Research (BeGenDiv) , Berlin, Germany
                Evolutionary Genetics Department, Leibniz-Institut für Zoo- und Wildtierforschung (IZW) , Berlin, Germany
                Author notes

                Maximilian Driller and Thomas Brown contributed equally to this work.

                To whom correspondence should be addressed. Tel. +493083859960. Email: mazzoni@ 123456izw-berlin.de
                Author information
                https://orcid.org/0000-0001-8293-4816
                https://orcid.org/0000-0003-3024-1449
                https://orcid.org/0000-0002-0706-3974
                Article
                dsae018
                10.1093/dnares/dsae018
                11215541
                38847751
                683e402c-d7b3-48aa-a23b-802337a599f4
                © The Author(s) 2024. Published by Oxford University Press on behalf of Kazusa DNA Research Institute.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License ( https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact reprints@oup.com for reprints and translation rights for reprints. All other permissions can be obtained through our RightsLink service via the Permissions link on the article page on our site—for further information please contact journals.permissions@oup.com.

                History
                : 02 February 2024
                : 18 April 2024
                : 06 June 2024
                : 01 July 2024
                Page count
                Pages: 9
                Categories
                Resource Article: Genomes Explored
                AcademicSubjects/MED00774
                AcademicSubjects/SCI01140
                AcademicSubjects/SCI01140

                Genetics
                genome assembly,genome annotation,pacbio,hi-c,pipistrellus nathusii
                Genetics
                genome assembly, genome annotation, pacbio, hi-c, pipistrellus nathusii

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