Illumina Genome Analyzer II paired end sequencing - SRA

ERX2008682: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 779,672 spots, 89.7M bases, 39.9Mb downloads

Design: Illumina sequencing of library NT201663P, constructed from sample accession ERS002157 for study accession ERP000150. This is part of an Illumina multiplexed sequencing run (4351_1). This submission includes reads tagged with the sequence TGACCA.

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

SAMEA734674 • ERS002157 • All experiments • All runs

Organism: Staphylococcus aureus

Library:

Name: NT201663P

Instrument: Illumina Genome Analyzer II

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Standard

Runs: 1 run, 779,672 spots, 89.7M bases, 39.9Mb

Run	# of Spots	# of Bases	Size	Published
ERR017174	779,672	89.7M	39.9Mb	2011-03-18

ID:: 3971825

SRA

Sequence Read Archive

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