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SRX20674929: Sequence capture of UCEs for Beloniscus sp.
1 ILLUMINA (Illumina NovaSeq 6000) run: 6M spots, 1.8G bases, 644.7Mb downloads

Design: UCE libraries were prepared using the KAPA Hyper Prep Kit (Kapa Biosystems), using up to 250 ng DNA (i.e., half reaction of manufacturers protocol) as starting material. Ampure XP beads were used for all cleanup steps. For samples containing <250 ng total, all DNA was used in library preparation. Target enrichment was performed on pooled libraries using the MYbaits Arachnida 1.1K version 1 kit (Arbor Biosciences, Ann Arbor, MI) following the Target Enrichment of Illumina Libraries v. 1.5 protocol (http://ultraconserved.org/#protocols). Hybridization was conducted at either 60 or 65 C for 24 hours, with a post-hybridization amplification of 18 cycles. Following an additional cleanup, libraries were quantified using a Qubit fluorometer and equimolar mixes were prepared for sequencing.
Submitted by: Harvard University
Study: Raw read data from multiple Opiliones libraries enriched for ultraconserved elements shared among Opiliones Raw sequence reads
show Abstracthide Abstract
Sequence capture of ultraconserved elements (UCEs) has transformed molecular systematics across many taxa, with arachnids being no exception. The probe set available for Arachnida has been repeatedly used across multiple arachnid lineages and taxonomic levels, however more specific probe sets for spiders have demonstrated that more UCEs can be recovered with higher probe specificity. In this study, we develop an Opiliones-specific UCE probe set targeting 1915 UCEs using a combination of probes designed from genomes and transcriptomes, as well as the most useful probes from the Arachnida probe set. We demonstrate the effectiveness of this probe set across Opiliones with the most complete family-level phylogeny made to date, including representatives from 61 of 63 currently described families. We also pay specific attention to UCE recovery from historical specimens with degraded DNA, population-level data sets, and assess backwards compatibility with samples hybridized with the Arachnida probe set. The resulting phylogenies - which include specimens hybridized using both the Opiliones and Arachnida probe sets, historical specimens, and transcriptomes - are largely congruent with previous multi-locus and phylogenomic analyses. The probe set is also backwards compatible, increasing the number of loci obtained in samples previously hybridized with the Arachnida probe set, and shows high utility down to shallow population-level divergences. This probe set has the potential to further transform Opiliones molecular systematics, resolving many long-standing taxonomic issues plaguing this lineage.
Sample:
SAMN35540755 • SRS17970538 • All experiments • All runs
Organism: Beloniscus sp.
Library:
Name: Beloniscus_sp_MCZ:IZ:37641
Instrument: Illumina NovaSeq 6000
Strategy: Targeted-Capture
Source: GENOMIC
Selection: Hybrid Selection
Layout: PAIRED
Runs: 1 run, 6M spots, 1.8G bases, 644.7Mb
Run# of Spots# of BasesSizePublished
SRR249138976,021,6481.8G644.7Mb2023-10-01

ID:
28104495

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