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ERX1995805: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 63,506 spots, 14.2M bases, 8.4Mb downloads

Design: Illumina sequencing of library NT204302F, constructed from sample accession ERS005831 for study accession ERP000157. This is part of an Illumina multiplexed sequencing run (4880_3). This submission includes reads tagged with the sequence CTTGTA.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Clostridium difficile ribotype 078 resequencing
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For further information on this study please see http://www.sanger.ac.uk/resources/downloads/bacteria/clostridium-difficile.html
Sample:
SAMEA742874 • ERS005831 • All experiments • All runs
Library:
Name: NT204302F
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 63,506 spots, 14.2M bases, 8.4Mb
Run# of Spots# of BasesSizePublished
ERR02733963,50614.2M8.4Mb2011-03-18

ID:
3942418

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