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ERX1995822: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 2.1M spots, 481.3M bases, 279.3Mb downloads

Design: Illumina sequencing of library NT206860P, constructed from sample accession ERS007222 for study accession ERP000159. This is part of an Illumina multiplexed sequencing run (4880_7). This submission includes reads tagged with the sequence ACAGTGGT.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Clostridium difficile ribotype 017 project
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For further information on this study please see http://www.sanger.ac.uk/resources/downloads/bacteria/clostridium-difficile.html
Sample: 4880_7#5
SAMEA708422 • ERS007222 • All experiments • All runs
Library:
Name: NT206860P
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 2.1M spots, 481.3M bases, 279.3Mb
Run# of Spots# of BasesSizePublished
ERR0273822,148,507481.3M279.3Mb2011-03-18

ID:
3942435

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