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ezRAD: a simplified method for genomic genotyping in non-model organisms

Here, we introduce ezRAD, a novel strategy for restriction site–associated DNA (RAD) that requires little technical expertise or investment in laboratory equipment, and demonstrate its utility for ten non-model organisms across a wide taxonomic range. ezRAD differs from other RAD methods primarily t...

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Autores principales: Toonen, Robert J., Puritz, Jonathan B., Forsman, Zac H., Whitney, Jonathan L., Fernandez-Silva, Iria, Andrews, Kimberly R., Bird, Christopher E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: PeerJ Inc. 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840413/
https://www.ncbi.nlm.nih.gov/pubmed/24282669
http://dx.doi.org/10.7717/peerj.203
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author Toonen, Robert J.
Puritz, Jonathan B.
Forsman, Zac H.
Whitney, Jonathan L.
Fernandez-Silva, Iria
Andrews, Kimberly R.
Bird, Christopher E.
author_facet Toonen, Robert J.
Puritz, Jonathan B.
Forsman, Zac H.
Whitney, Jonathan L.
Fernandez-Silva, Iria
Andrews, Kimberly R.
Bird, Christopher E.
author_sort Toonen, Robert J.
collection PubMed
description Here, we introduce ezRAD, a novel strategy for restriction site–associated DNA (RAD) that requires little technical expertise or investment in laboratory equipment, and demonstrate its utility for ten non-model organisms across a wide taxonomic range. ezRAD differs from other RAD methods primarily through its use of standard Illumina TruSeq library preparation kits, which makes it possible for any laboratory to send out to a commercial genomic core facility for library preparation and next-generation sequencing with virtually no additional investment beyond the cost of the service itself. This simplification opens RADseq to any lab with the ability to extract DNA and perform a restriction digest. ezRAD also differs from others in its flexibility to use any restriction enzyme (or combination of enzymes) that cuts frequently enough to generate fragments of the desired size range, without requiring the purchase of separate adapters for each enzyme or a sonication step, which can further decrease the cost involved in choosing optimal enzymes for particular species and research questions. We apply this method across a wide taxonomic diversity of non-model organisms to demonstrate the utility and flexibility of our approach. The simplicity of ezRAD makes it particularly useful for the discovery of single nucleotide polymorphisms and targeted amplicon sequencing in natural populations of non-model organisms that have been historically understudied because of lack of genomic information.
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spelling pubmed-38404132013-11-26 ezRAD: a simplified method for genomic genotyping in non-model organisms Toonen, Robert J. Puritz, Jonathan B. Forsman, Zac H. Whitney, Jonathan L. Fernandez-Silva, Iria Andrews, Kimberly R. Bird, Christopher E. PeerJ Genetics Here, we introduce ezRAD, a novel strategy for restriction site–associated DNA (RAD) that requires little technical expertise or investment in laboratory equipment, and demonstrate its utility for ten non-model organisms across a wide taxonomic range. ezRAD differs from other RAD methods primarily through its use of standard Illumina TruSeq library preparation kits, which makes it possible for any laboratory to send out to a commercial genomic core facility for library preparation and next-generation sequencing with virtually no additional investment beyond the cost of the service itself. This simplification opens RADseq to any lab with the ability to extract DNA and perform a restriction digest. ezRAD also differs from others in its flexibility to use any restriction enzyme (or combination of enzymes) that cuts frequently enough to generate fragments of the desired size range, without requiring the purchase of separate adapters for each enzyme or a sonication step, which can further decrease the cost involved in choosing optimal enzymes for particular species and research questions. We apply this method across a wide taxonomic diversity of non-model organisms to demonstrate the utility and flexibility of our approach. The simplicity of ezRAD makes it particularly useful for the discovery of single nucleotide polymorphisms and targeted amplicon sequencing in natural populations of non-model organisms that have been historically understudied because of lack of genomic information. PeerJ Inc. 2013-11-19 /pmc/articles/PMC3840413/ /pubmed/24282669 http://dx.doi.org/10.7717/peerj.203 Text en © 2013 Toonen et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Genetics
Toonen, Robert J.
Puritz, Jonathan B.
Forsman, Zac H.
Whitney, Jonathan L.
Fernandez-Silva, Iria
Andrews, Kimberly R.
Bird, Christopher E.
ezRAD: a simplified method for genomic genotyping in non-model organisms
title ezRAD: a simplified method for genomic genotyping in non-model organisms
title_full ezRAD: a simplified method for genomic genotyping in non-model organisms
title_fullStr ezRAD: a simplified method for genomic genotyping in non-model organisms
title_full_unstemmed ezRAD: a simplified method for genomic genotyping in non-model organisms
title_short ezRAD: a simplified method for genomic genotyping in non-model organisms
title_sort ezrad: a simplified method for genomic genotyping in non-model organisms
topic Genetics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3840413/
https://www.ncbi.nlm.nih.gov/pubmed/24282669
http://dx.doi.org/10.7717/peerj.203
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