15
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      A novel method of microsatellite genotyping-by-sequencing using individual combinatorial barcoding

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          This study examines the potential of next-generation sequencing based ‘genotyping-by-sequencing’ (GBS) of microsatellite loci for rapid and cost-effective genotyping in large-scale population genetic studies. The recovery of individual genotypes from large sequence pools was achieved by PCR-incorporated combinatorial barcoding using universal primers. Three experimental conditions were employed to explore the possibility of using this approach with existing and novel multiplex marker panels and weighted amplicon mixture. The GBS approach was validated against microsatellite data generated by capillary electrophoresis. GBS allows access to the underlying nucleotide sequences that can reveal homoplasy, even in large datasets and facilitates cross laboratory transfer. GBS of microsatellites, using individual combinatorial barcoding, is potentially faster and cheaper than current microsatellite approaches and offers better and more data.

          Related collections

          Most cited references30

          • Record: found
          • Abstract: found
          • Article: not found

          An integrated semiconductor device enabling non-optical genome sequencing.

          The seminal importance of DNA sequencing to the life sciences, biotechnology and medicine has driven the search for more scalable and lower-cost solutions. Here we describe a DNA sequencing technology in which scalable, low-cost semiconductor manufacturing techniques are used to make an integrated circuit able to directly perform non-optical DNA sequencing of genomes. Sequence data are obtained by directly sensing the ions produced by template-directed DNA polymerase synthesis using all-natural nucleotides on this massively parallel semiconductor-sensing device or ion chip. The ion chip contains ion-sensitive, field-effect transistor-based sensors in perfect register with 1.2 million wells, which provide confinement and allow parallel, simultaneous detection of independent sequencing reactions. Use of the most widely used technology for constructing integrated circuits, the complementary metal-oxide semiconductor (CMOS) process, allows for low-cost, large-scale production and scaling of the device to higher densities and larger array sizes. We show the performance of the system by sequencing three bacterial genomes, its robustness and scalability by producing ion chips with up to 10 times as many sensors and sequencing a human genome.
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found
            Is Open Access

            The complete genome of an individual by massively parallel DNA sequencing.

            The association of genetic variation with disease and drug response, and improvements in nucleic acid technologies, have given great optimism for the impact of 'genomic medicine'. However, the formidable size of the diploid human genome, approximately 6 gigabases, has prevented the routine application of sequencing methods to deciphering complete individual human genomes. To realize the full potential of genomics for human health, this limitation must be overcome. Here we report the DNA sequence of a diploid genome of a single individual, James D. Watson, sequenced to 7.4-fold redundancy in two months using massively parallel sequencing in picolitre-size reaction vessels. This sequence was completed in two months at approximately one-hundredth of the cost of traditional capillary electrophoresis methods. Comparison of the sequence to the reference genome led to the identification of 3.3 million single nucleotide polymorphisms, of which 10,654 cause amino-acid substitution within the coding sequence. In addition, we accurately identified small-scale (2-40,000 base pair (bp)) insertion and deletion polymorphism as well as copy number variation resulting in the large-scale gain and loss of chromosomal segments ranging from 26,000 to 1.5 million base pairs. Overall, these results agree well with recent results of sequencing of a single individual by traditional methods. However, in addition to being faster and significantly less expensive, this sequencing technology avoids the arbitrary loss of genomic sequences inherent in random shotgun sequencing by bacterial cloning because it amplifies DNA in a cell-free system. As a result, we further demonstrate the acquisition of novel human sequence, including novel genes not previously identified by traditional genomic sequencing. This is the first genome sequenced by next-generation technologies. Therefore it is a pilot for the future challenges of 'personalized genome sequencing'.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Current trends in microsatellite genotyping.

              Microsatellites have been popular molecular markers ever since their advent in the late eighties. Despite growing competition from new genotyping and sequencing techniques, the use of these versatile and cost-effective markers continues to increase, boosted by successive technical advances. First, methods for multiplexing PCR have considerably improved over the last years, thereby decreasing genotyping costs and increasing throughput. Second, next-generation sequencing technologies allow the identification of large numbers of microsatellite loci at reduced cost in non-model species. As a consequence, more stringent selection of loci is possible, thereby further enhancing multiplex quality and efficiency. However, current practices are lagging behind. By surveying recently published population genetic studies relying on simple sequence repeats, we show that more than half of the studies lack appropriate quality controls and do not make use of multiplex PCR. To make the most of the latest technical developments, we outline the need for a well-established strategy including standardized high-throughput bench protocols and specific bioinformatic tools, from primer design to allele calling. © 2011 Blackwell Publishing Ltd.
                Bookmark

                Author and article information

                Journal
                R Soc Open Sci
                R Soc Open Sci
                RSOS
                royopensci
                Royal Society Open Science
                The Royal Society Publishing
                2054-5703
                January 2016
                20 January 2016
                20 January 2016
                : 3
                : 1
                : 150565
                Affiliations
                [1 ]Area 52 Research Group, University College Dublin , Belfield, Dublin, Republic of Ireland
                [2 ]School of Biology and Environment Science, University College Dublin , Belfield, Dublin, Republic of Ireland
                [3 ]Earth Institute, University College Dublin , Belfield, Dublin, Republic of Ireland
                [4 ]Carna Research Station, Ryan Institute, National University of Ireland , Galway, Carna, Connemara, Republic of Ireland
                [5 ]Evolutionary Genomics Group, Research Programme on Biomedical Informatics (GRIB) , Hospital del Mar Research Institute (IMIM), Universitat Pompeu Fabra (UPF), Barcelona 08003, Spain
                [6 ]School of Biological Sciences, Queen’s University Belfast , Medical Biology Centre, Lisburn Road, Belfast, UK
                [7 ]Department of Biological Sciences, Old Dominion University , Norfolk, VA, USA
                [8 ]Beaufort Fish Genetics Programme, School of Biological , Earth and Environmental Sciences/Aquaculture and Fisheries Development Centre, University College Cork, Distillery Fields, North Mall, Cork, Republic of Ireland
                [9 ]Marine and Freshwater Research Centre, Galway-Mayo Institute of Technology , Dublin Road, Galway, Republic of Ireland
                [10 ]Teagasc Food Research Centre , Moorepark, Fermoy, Cork, Republic of Ireland
                [11 ]Alimentary Pharmabiotic Centre , Cork, Republic of Ireland
                Author notes
                Author for correspondence: Salla Vartia e-mail: salla.vartia@ 123456gmail.com
                Author information
                http://orcid.org/0000-0001-5704-2883
                Article
                rsos150565
                10.1098/rsos.150565
                4736940
                26909185
                470355c5-59a7-46b6-8acd-9cebf3afb8fe

                © 2016 The Authors. Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.

                History
                : 21 October 2015
                : 10 December 2015
                Funding
                Funded by: Marine Institute and the Marine Research Sub-programme of the National Development Plan 2007-2013, co-financed by the European Regional Development Fund
                Award ID: PBA/AF/07/004
                Funded by: Science Foundation Ireland http://dx.doi.org/10.13039/501100001602
                Award ID: SFI 12/IP/1308
                Funded by: Irish Research Council (IRC) Graduate Research Education Programme (GREP)
                Funded by: Spanish Ministerio de Economía y Competitividad
                Award ID: FPI BES-2010-038494 and EEBB-I-13-06270
                Funded by: Beaufort Marine Research Award in Fish Population Genetics funded by the Irish Government under the Sea Change Programme
                Funded by: Irish Research Council (IRC)
                Award ID: GOIPD/2013/320
                Categories
                1001
                197
                198
                60
                Genetics
                Research Article
                Custom metadata
                January, 2016

                amplicon sequencing,gadus morhua,genotyping by sequencing,next-generation sequencing,ssr,universal primer

                Comments

                Comment on this article