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SRX20527431: ddRADSeq of Poecilimon luschani: muscle
1 ILLUMINA (Illumina HiSeq 2500) run: 3.1M spots, 438.3M bases, 237Mb downloads

Design: We used Qiagen DNeasy kits (Qiagen, Hilden, Germany) to extract and purify genomic DNA from the hind femur of each individual. We processed genomic DNA into one genomic library (100 individuals/library) using the double-digestion restriction-site associated DNA sequencing procedure (ddRAD-seq) described in Peterson et al. (2012) (PLOS One, 7: e37135). In brief, we digested DNA with the restriction enzymes MseI and EcoRI (New England Biolabs, Ipswich, MA, USA) and ligated Illumina adaptors including unique 11-bp barcodes to the digested fragments of each individual. We pooled ligation products and size-selected them between 350-450 bp with a Pippin Prep machine (Sage Science, Beverly, MA, USA). We amplified the fragments by PCR with 12 cycles using the iProofTM High-Fidelity DNA Polymerase (BIO-RAD, Hercules, CA, USA) and sequenced the library in two single-read 150-bp lanes on an Illumina HiSeq2500 platform at The Centre for Applied Genomics (SickKids, Toronto, ON, Canada).
Submitted by: Estacion Biologica de Donana (EBD-CSIC)
Study: RADseq for Poecilimon (Orthoptera: Tettigoniidae)
show Abstracthide Abstract
The goal of this project is to use next generation sequencing (NGS) data to resolve taxonomic uncertainties and infer the demographic processes underlying the diversification of bush crickets from the genus Poecilimon (Orthoptera: Tettigoniidae).
Sample:
SAMN35443022 • SRS17836720 • All experiments • All runs
Library:
Name: PLulGele06
Instrument: Illumina HiSeq 2500
Strategy: RAD-Seq
Source: GENOMIC
Selection: Restriction Digest
Layout: SINGLE
Runs: 1 run, 3.1M spots, 438.3M bases, 237Mb
Run# of Spots# of BasesSizePublished
SRR247512503,130,461438.3M237Mb2023-10-26

ID:
27951140

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