Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).

Transcriptome-based exon capture approaches, along with next-generation sequencing, are allowing for the rapid and cost-effective production of extensive and informative phylogenomic datasets from non-model organisms for phylogenetics and population genetics research. These approaches generally empl...

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Autores principales: Danielle N Stringer, Terry Bertozzi, Karen Meusemann, Steven Delean, Michelle T Guzik, Simon M Tierney, Christoph Mayer, Steven J B Cooper, Mohammad Javidkar, Andreas Zwick, Andrew D Austin
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Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/c18d713e7e274d9aa5dd419474a275c4
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spelling oai:doaj.org-article:c18d713e7e274d9aa5dd419474a275c42021-12-02T20:14:33ZDevelopment and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).1932-620310.1371/journal.pone.0256861https://doaj.org/article/c18d713e7e274d9aa5dd419474a275c42021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0256861https://doaj.org/toc/1932-6203Transcriptome-based exon capture approaches, along with next-generation sequencing, are allowing for the rapid and cost-effective production of extensive and informative phylogenomic datasets from non-model organisms for phylogenetics and population genetics research. These approaches generally employ a reference genome to infer the intron-exon structure of targeted loci and preferentially select longer exons. However, in the absence of an existing and well-annotated genome, we applied this exon capture method directly, without initially identifying intron-exon boundaries for bait design, to a group of highly diverse Haloniscus (Philosciidae), paraplatyarthrid and armadillid isopods, and examined the performance of our methods and bait design for phylogenetic inference. Here, we identified an isopod-specific set of single-copy protein-coding loci, and a custom bait design to capture targeted regions from 469 genes, and analysed the resulting sequence data with a mapping approach and newly-created post-processing scripts. We effectively recovered a large and informative dataset comprising both short (<100 bp) and longer (>300 bp) exons, with high uniformity in sequencing depth. We were also able to successfully capture exon data from up to 16-year-old museum specimens along with more distantly related outgroup taxa, and efficiently pool multiple samples prior to capture. Our well-resolved phylogenies highlight the overall utility of this methodological approach and custom bait design, which offer enormous potential for application to future isopod, as well as broader crustacean, molecular studies.Danielle N StringerTerry BertozziKaren MeusemannSteven DeleanMichelle T GuzikSimon M TierneyChristoph MayerSteven J B CooperMohammad JavidkarAndreas ZwickAndrew D AustinPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 9, p e0256861 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Danielle N Stringer
Terry Bertozzi
Karen Meusemann
Steven Delean
Michelle T Guzik
Simon M Tierney
Christoph Mayer
Steven J B Cooper
Mohammad Javidkar
Andreas Zwick
Andrew D Austin
Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
description Transcriptome-based exon capture approaches, along with next-generation sequencing, are allowing for the rapid and cost-effective production of extensive and informative phylogenomic datasets from non-model organisms for phylogenetics and population genetics research. These approaches generally employ a reference genome to infer the intron-exon structure of targeted loci and preferentially select longer exons. However, in the absence of an existing and well-annotated genome, we applied this exon capture method directly, without initially identifying intron-exon boundaries for bait design, to a group of highly diverse Haloniscus (Philosciidae), paraplatyarthrid and armadillid isopods, and examined the performance of our methods and bait design for phylogenetic inference. Here, we identified an isopod-specific set of single-copy protein-coding loci, and a custom bait design to capture targeted regions from 469 genes, and analysed the resulting sequence data with a mapping approach and newly-created post-processing scripts. We effectively recovered a large and informative dataset comprising both short (<100 bp) and longer (>300 bp) exons, with high uniformity in sequencing depth. We were also able to successfully capture exon data from up to 16-year-old museum specimens along with more distantly related outgroup taxa, and efficiently pool multiple samples prior to capture. Our well-resolved phylogenies highlight the overall utility of this methodological approach and custom bait design, which offer enormous potential for application to future isopod, as well as broader crustacean, molecular studies.
format article
author Danielle N Stringer
Terry Bertozzi
Karen Meusemann
Steven Delean
Michelle T Guzik
Simon M Tierney
Christoph Mayer
Steven J B Cooper
Mohammad Javidkar
Andreas Zwick
Andrew D Austin
author_facet Danielle N Stringer
Terry Bertozzi
Karen Meusemann
Steven Delean
Michelle T Guzik
Simon M Tierney
Christoph Mayer
Steven J B Cooper
Mohammad Javidkar
Andreas Zwick
Andrew D Austin
author_sort Danielle N Stringer
title Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
title_short Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
title_full Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
title_fullStr Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
title_full_unstemmed Development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (Philosciidae: Haloniscus).
title_sort development and evaluation of a custom bait design based on 469 single-copy protein-coding genes for exon capture of isopods (philosciidae: haloniscus).
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/c18d713e7e274d9aa5dd419474a275c4
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