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SRX555711: Aporus niger UCE
1 ILLUMINA (Illumina MiSeq) run: 205,167 spots, 103M bases, 52.8Mb downloads

Design: Randomly sheared DNA to a target size of approximately 650 bp (range 400-800 bp) by sonication (Qsonica Inc. Q800 or Diagenode BioRuptor), and we input 50-500 ng sheared DNA (418 ng mean) into a modified genomic DNA library preparation protocol (Kapa Biosystems) that incorporated "with-bead" cleanup steps (Fisher et al. 2011) using a generic SPRI substitute ((Rohland & Reich 2012); hereafter SPRI). This protocol is similar to the Kapa Biosystems protocol that uses commercial SPRI chemistry for cleanup and includes end-repair, adenylation, and T/A ligation steps, except that the Fisher modification does not remove and replace SPRI beads between each step. We also substituted custom-designed sequence-tagged adapters to the ligation reaction (Faircloth & Glenn 2012).
Submitted by: UNIVERSITY OF CALIFORNIA
Study: Hymenopteran UCE sequences
show Abstracthide Abstract
Gaining a genomic perspective on phylogeny requires the collection of data from many putatively independent loci collected across the genome. Among insects, a primary approach to collecting this class of data involves transcriptome sequencing, because few insects have high-quality genome sequences available; assembling new genomes remains a limiting factor; the transcribed portion of the genome is a reasonable, reduced subset of the genome to target; and the data collected from transcribed portions of the genome are similar in composition to the types of data with which biologists have traditionally worked (e.g. exons). However, molecular techniques requiring RNA as a template, including transcriptome sequencing, are limited to using very high quality source materials, which are often unavailable from a large proportion of biologically important insect samples. Recent research suggests that DNA-based target enrichment of conserved genomic elements offers another path to collecting phylogenomic data across insect taxa, provided that conserved elements are present in and can be collected from insect genomes. Here, we identify a large set (n=1,510) of ultraconserved elements (UCE) shared among the insect order Hymenoptera. We use in silico analyses to show that these loci accurately reconstruct relationships among genome-enabled Hymenoptera, and we design a set of baits for enriching these loci that researchers can use with DNA templates extracted from a variety of sources. We use our UCE bait set to enrich an average of 720 UCE loci from 30 hymenopteran taxa, and we use these UCE loci to reconstruct phylogenetic relationships spanning very old (=220 MYA) to very young (=1 MYA) divergences among hymenopteran lineages. In contrast to a recent study addressing hymenopteran phylogeny using transcriptome data, we found ants to be sister to all remaining aculeate lineages with complete support. We discuss this approach and our results in the context of elucidating the evolutionary history of one of the most diverse and speciose animal orders.
Sample: MIGS Eukaryotic sample from Aporus niger
SAMN02803937 • SRS622799 • All experiments • All runs
Organism: Aporus niger
Library:
Name: Aporus niger
Instrument: Illumina MiSeq
Strategy: WGS
Source: GENOMIC
Selection: Hybrid Selection
Layout: PAIRED
Spot descriptor:
forward251  reverse

Experiment attributes:
index: BFIDT-020:TAAGAGCGCC
Pipeline: show...hide...
Program
MiSeq Basespace
Runs: 1 run, 205,167 spots, 103M bases, 52.8Mb
Run# of Spots# of BasesSizePublished
SRR1303319205,167103M52.8Mb2014-05-31

ID:
794739

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