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SRX3384047: RAD-seq of Pungitius hellenicus: female
1 ILLUMINA (Illumina HiSeq 2000) run: 3.7M spots, 727.1M bases, 522.9Mb downloads

Design: Genomic DNA was extracted from ethanol preserved fin clips or muscle tissue using the standard phenol-chloroform method. Approximately 100 ng of genomic DNA was isolated for RAD library construction following the protocol of Baird et al. (2008). DNA was fragmented with restriction enzyme (PstI). P1 adapter with forward amplification and sequencing primers and sample specific barcode were ligated to the digested DNA fragments. Barcoded samples were sheared randomly and the P2 adapter was added. DNA fragments of 300 to 500 bp in length were gel purified after selective PCR enrichment step. Barcoded RAD samples were then pooled and sequenced using the Illumina HiSeq2000 platform with 100 bp paired-end strategy.
Submitted by: Institute of Zoology, Chinese Academy of Science
Study: Pungitius RAD-seq sequencing
show Abstracthide Abstract
The global Pungitius stickleback evolutionary study.
Sample:
SAMN08013781 • SRS2679417 • All experiments • All runs
Library:
Name: G786
Instrument: Illumina HiSeq 2000
Strategy: RAD-Seq
Source: GENOMIC
Selection: Restriction Digest
Layout: PAIRED
Runs: 1 run, 3.7M spots, 727.1M bases, 522.9Mb
Run# of Spots# of BasesSizePublished
SRR62819803,709,830727.1M522.9Mb2020-12-31

ID:
4721751

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