4.7 Article

Effective double-digest RAD sequencing and genotyping despite large genome size

Journal

MOLECULAR ECOLOGY RESOURCES
Volume 21, Issue 4, Pages 1037-1055

Publisher

WILEY
DOI: 10.1111/1755-0998.13314

Keywords

Cypripedium calceolus; ddRADseq; lady's slipper orchid; large genome; population genetics; SNPs

Funding

  1. Estonian Ministry of Education and Research [IUT 21-1]
  2. British Ecological Society [SR18/1418]
  3. Kew Pilot Study Fund 2018

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The study aims to bridge the gap between the applicability of RAD sequencing in nonmodel plants with large genomes and the use of loci for population genetic inference. It provides a complete workflow from library preparation to genetic diversity and differentiation inference, emphasizing the importance of quality checks and filtering strategies. The study highlights the necessity of exploring and adapting filtering strategies to dismiss potentially misleading data and not neglecting the occurrence of organellar sequences in libraries for reliable results.
Obtaining informative data is the ambition of any genomic project, but in nonmodel species with very large genomes, pursuing such a goal requires surmounting a series of analytical challenges. Double-digest RAD sequencing is routinely used in nonmodel organisms and offers some control over the volume of data obtained. However, the volume of data recovered is not always an indication of the reliability of data sets, and quality checks are necessary to ensure that true and artefactual information is set apart. In the present study, we aim to fill the gap existing between the known applicability of RAD sequencing methods in plants with large genomes and the use of the retrieved loci for population genetic inference. By analysing two populations of Cypripedium calceolus, a nonmodel orchid species with a large genome size (1C similar to 31.6 Gbp), we provide a complete workflow from library preparation to bioinformatic filtering and inference of genetic diversity and differentiation. We show how filtering strategies to dismiss potentially misleading data need to be explored and adapted to data set-specific features. Moreover, we suggest that the occurrence of organellar sequences in libraries should not be neglected when planning the experiment and analysing the results. Finally, we explain how, in the absence of prior information about the genome of the species, seeking high standards of quality during library preparation and sequencing can provide an insurance against unpredicted technical or biological constraints.

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