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ERX1627953: Illumina HiSeq 2000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2000) run: 1.2M spots, 291.6M bases, 92.9Mb downloads

Design: Illumina sequencing of library 16539773, constructed from sample accession ERS1080767 for study accession ERP014470. This is part of an Illumina multiplexed sequencing run (19789_6). This submission includes reads tagged with the sequence GAGGTGCTATAGAGGC.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: WTTGseq
PRJEB12937 • ERP014470 • All experiments • All runs
show Abstracthide Abstract
The study is to investigate the hypothesis that WGS will determine the origin of VREfm in a cohort of hospitalised patients. Specifically to determine whether VREfm is solely acquired through nosocomial transmission, or if a proportion can be attributed to gut flora already present at initial presentation.
Sample: 19789_6#168
SAMEA3893633 • ERS1080767 • All experiments • All runs
Organism: Enterococcus faecium
Library:
Name: 16539773
Instrument: Illumina HiSeq 2000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 1.2M spots, 291.6M bases, 92.9Mb
Run# of Spots# of BasesSizePublished
ERR15571971,166,293291.6M92.9Mb2016-08-05

ID:
2884282

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