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ERX2006284: Illumina Genome Analyzer II paired end sequencing
1 ILLUMINA (Illumina Genome Analyzer II) run: 1.8M spots, 404.8M bases, 262.8Mb downloads

Design: Illumina sequencing of library NT206882V, constructed from sample accession ERS007231 for study accession ERP000145. This is part of an Illumina multiplexed sequencing run (4880_8). This submission includes reads tagged with the sequence CGATGTTT.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Mycobacterium microti genome diversity project
PRJEB2091 • ERP000145 • All experiments • All runs
show Abstracthide Abstract
For further information on this study please see http://www.sanger.ac.uk/resources/downloads/bacteria/mycobacterium.html
Sample:
SAMEA806953 • ERS007231 • All experiments • All runs
Organism: Mycobacterium tuberculosis variant microti
Library:
Name: NT206882V
Instrument: Illumina Genome Analyzer II
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 1.8M spots, 404.8M bases, 262.8Mb
Run# of Spots# of BasesSizePublished
ERR0272951,807,245404.8M262.8Mb2011-03-18

ID:
3965911

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