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ERX415713: Illumina HiSeq 2000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2000) run: 3.1M spots, 612M bases, 297.4Mb downloads

Design: Illumina sequencing of library 8967058, constructed from sample accession ERS366983 for study accession ERP001857. This is part of an Illumina multiplexed sequencing run (11822_8). This submission includes reads tagged with the sequence TGCATAGT.
Submitted by: The Wellcome Trust Sanger Institute (SC)
Study: Streptococcus_pyogenes_infections_among_children_admitted_to_Kilifi_District_Hospital
show Abstracthide Abstract
www.sanger.ac.uk/resources/downloads/bacteria/s-pyogenes
Sample: 11822_8#23
SAMEA2238171 • ERS366983 • All experiments • All runs
Library:
Name: 8967058
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 3.1M spots, 612M bases, 297.4Mb
Run# of Spots# of BasesSizePublished
ERR4493413,060,135612M297.4Mb2014-05-14

ID:
743473

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