Data from: Targeted re-sequencing of coding DNA sequences for SNP discovery in non-model species ...

Targeted capture coupled with high throughput sequencing can be used to gain information about nuclear sequence variation at hundreds to thousands of loci. Divergent reference capture makes use of molecular data of one species to enrich target loci in other (related) species. This is particularly va...

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Bibliographic Details
Main Authors: Förster, Daniel W., Bull, James K., Lenz, Dorina, Autenrieth, Marijke, Paijmans, Johanna L.A., Kraus, Robert H.S., Nowak, Carsten, Bayerl, Helmut, Kuehn, Ralph, Saveljev, Alexander P., Sindičić, Magda, Hofreiter, Michael, Schmidt, Krzysztof, Fickel, Joerns, Paijmans, Johanna L. A., Kraus, Robert H. S.
Format: Dataset
Language:English
Published: Dryad 2018
Subjects:
CDS
Online Access:https://dx.doi.org/10.5061/dryad.3f4jr01
https://datadryad.org/stash/dataset/doi:10.5061/dryad.3f4jr01
Description
Summary:Targeted capture coupled with high throughput sequencing can be used to gain information about nuclear sequence variation at hundreds to thousands of loci. Divergent reference capture makes use of molecular data of one species to enrich target loci in other (related) species. This is particularly valuable for non-model organisms, for which often no a priori knowledge exists regarding these loci. Here, we have used targeted capture to obtain data for 809 nuclear coding DNA sequences (CDS) in a non-model organism, the Eurasian lynx Lynx lynx, using baits designed with the help of the published genome of a related model organism (the domestic cat Felis catus). Using this approach, we were able to survey intraspecific variation at hundreds of nuclear loci in L. lynx across the species’ European range. A large set of bi-allelic candidate SNPs was then evaluated using a high throughput SNP-genotyping platform (Fluidigm), which we then reduced to a final 96 SNP-panel based on assay performance and reliability; ... : CDS-baits and SNP dataThis ZIP folder contains bait sequences (FASTA), the 96 SNP-panel, SNP genotypes (Illumina and Fluidigm), and an R script. Details can be found in the READ ME file.DRYAD.zip ...