Cargando…

Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing

BACKGROUND: Genome-wide data are invaluable to characterize differentiation and adaptation of natural populations. Reduced representation sequencing (RRS) subsamples a genome repeatedly across many individuals. However, RRS requires careful optimization and fine-tuning to deliver high marker density...

Descripción completa

Detalles Bibliográficos
Autores principales: Christiansen, Henrik, Heindler, Franz M., Hellemans, Bart, Jossart, Quentin, Pasotti, Francesca, Robert, Henri, Verheye, Marie, Danis, Bruno, Kochzius, Marc, Leliaert, Frederik, Moreau, Camille, Patel, Tasnim, Van de Putte, Anton P., Vanreusel, Ann, Volckaert, Filip A. M., Schön, Isa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380342/
https://www.ncbi.nlm.nih.gov/pubmed/34418978
http://dx.doi.org/10.1186/s12864-021-07917-3
_version_ 1783741178238205952
author Christiansen, Henrik
Heindler, Franz M.
Hellemans, Bart
Jossart, Quentin
Pasotti, Francesca
Robert, Henri
Verheye, Marie
Danis, Bruno
Kochzius, Marc
Leliaert, Frederik
Moreau, Camille
Patel, Tasnim
Van de Putte, Anton P.
Vanreusel, Ann
Volckaert, Filip A. M.
Schön, Isa
author_facet Christiansen, Henrik
Heindler, Franz M.
Hellemans, Bart
Jossart, Quentin
Pasotti, Francesca
Robert, Henri
Verheye, Marie
Danis, Bruno
Kochzius, Marc
Leliaert, Frederik
Moreau, Camille
Patel, Tasnim
Van de Putte, Anton P.
Vanreusel, Ann
Volckaert, Filip A. M.
Schön, Isa
author_sort Christiansen, Henrik
collection PubMed
description BACKGROUND: Genome-wide data are invaluable to characterize differentiation and adaptation of natural populations. Reduced representation sequencing (RRS) subsamples a genome repeatedly across many individuals. However, RRS requires careful optimization and fine-tuning to deliver high marker density while being cost-efficient. The number of genomic fragments created through restriction enzyme digestion and the sequencing library setup must match to achieve sufficient sequencing coverage per locus. Here, we present a workflow based on published information and computational and experimental procedures to investigate and streamline the applicability of RRS. RESULTS: In an iterative process genome size estimates, restriction enzymes and size selection windows were tested and scaled in six classes of Antarctic animals (Ostracoda, Malacostraca, Bivalvia, Asteroidea, Actinopterygii, Aves). Achieving high marker density would be expensive in amphipods, the malacostracan target taxon, due to the large genome size. We propose alternative approaches such as mitogenome or target capture sequencing for this group. Pilot libraries were sequenced for all other target taxa. Ostracods, bivalves, sea stars, and fish showed overall good coverage and marker numbers for downstream population genomic analyses. In contrast, the bird test library produced low coverage and few polymorphic loci, likely due to degraded DNA. CONCLUSIONS: Prior testing and optimization are important to identify which groups are amenable for RRS and where alternative methods may currently offer better cost-benefit ratios. The steps outlined here are easy to follow for other non-model taxa with little genomic resources, thus stimulating efficient resource use for the many pressing research questions in molecular ecology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07917-3.
format Online
Article
Text
id pubmed-8380342
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-83803422021-08-23 Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing Christiansen, Henrik Heindler, Franz M. Hellemans, Bart Jossart, Quentin Pasotti, Francesca Robert, Henri Verheye, Marie Danis, Bruno Kochzius, Marc Leliaert, Frederik Moreau, Camille Patel, Tasnim Van de Putte, Anton P. Vanreusel, Ann Volckaert, Filip A. M. Schön, Isa BMC Genomics Research BACKGROUND: Genome-wide data are invaluable to characterize differentiation and adaptation of natural populations. Reduced representation sequencing (RRS) subsamples a genome repeatedly across many individuals. However, RRS requires careful optimization and fine-tuning to deliver high marker density while being cost-efficient. The number of genomic fragments created through restriction enzyme digestion and the sequencing library setup must match to achieve sufficient sequencing coverage per locus. Here, we present a workflow based on published information and computational and experimental procedures to investigate and streamline the applicability of RRS. RESULTS: In an iterative process genome size estimates, restriction enzymes and size selection windows were tested and scaled in six classes of Antarctic animals (Ostracoda, Malacostraca, Bivalvia, Asteroidea, Actinopterygii, Aves). Achieving high marker density would be expensive in amphipods, the malacostracan target taxon, due to the large genome size. We propose alternative approaches such as mitogenome or target capture sequencing for this group. Pilot libraries were sequenced for all other target taxa. Ostracods, bivalves, sea stars, and fish showed overall good coverage and marker numbers for downstream population genomic analyses. In contrast, the bird test library produced low coverage and few polymorphic loci, likely due to degraded DNA. CONCLUSIONS: Prior testing and optimization are important to identify which groups are amenable for RRS and where alternative methods may currently offer better cost-benefit ratios. The steps outlined here are easy to follow for other non-model taxa with little genomic resources, thus stimulating efficient resource use for the many pressing research questions in molecular ecology. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12864-021-07917-3. BioMed Central 2021-08-21 /pmc/articles/PMC8380342/ /pubmed/34418978 http://dx.doi.org/10.1186/s12864-021-07917-3 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Christiansen, Henrik
Heindler, Franz M.
Hellemans, Bart
Jossart, Quentin
Pasotti, Francesca
Robert, Henri
Verheye, Marie
Danis, Bruno
Kochzius, Marc
Leliaert, Frederik
Moreau, Camille
Patel, Tasnim
Van de Putte, Anton P.
Vanreusel, Ann
Volckaert, Filip A. M.
Schön, Isa
Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title_full Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title_fullStr Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title_full_unstemmed Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title_short Facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
title_sort facilitating population genomics of non-model organisms through optimized experimental design for reduced representation sequencing
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8380342/
https://www.ncbi.nlm.nih.gov/pubmed/34418978
http://dx.doi.org/10.1186/s12864-021-07917-3
work_keys_str_mv AT christiansenhenrik facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT heindlerfranzm facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT hellemansbart facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT jossartquentin facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT pasottifrancesca facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT roberthenri facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT verheyemarie facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT danisbruno facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT kochziusmarc facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT leliaertfrederik facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT moreaucamille facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT pateltasnim facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT vandeputteantonp facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT vanreuselann facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT volckaertfilipam facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing
AT schonisa facilitatingpopulationgenomicsofnonmodelorganismsthroughoptimizedexperimentaldesignforreducedrepresentationsequencing