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ERX2008613: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 827,775 spots, 95.2M bases, 42.6Mb downloads

Design: Illumina sequencing of library NT201741M, constructed from sample accession ERS002224 for study accession ERP000150. This is part of an Illumina multiplexed sequencing run (4351_8). This submission includes reads tagged with the sequence TTAGGC.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Sequencing the genomes from a global sample of Staphylococcus aureus ST22
PRJEB2096 • ERP000150 • All experiments • All runs
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For further information on this study please see http://www.sanger.ac.uk/resources/downloads/bacteria/staphylococcus-aureus.html
Sample: Staphylococcus aureus; Staphylococcus aureus
SAMEA734784 • ERS002224 • All experiments • All runs
Organism: Staphylococcus aureus
Library:
Name: NT201741M
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 827,775 spots, 95.2M bases, 42.6Mb
Run# of Spots# of BasesSizePublished
ERR017245827,77595.2M42.6Mb2011-03-18

ID:
3971756

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