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ERX2798241: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 3.4M spots, 845.1M bases, 294.3Mb downloads

Design: Illumina sequencing of library DN490184F:H10, constructed from sample accession ERS1810698 for study accession ERP011197. This is part of an Illumina multiplexed sequencing run (23612_1). This submission includes reads tagged with the sequence GTCGCTAT.
Submitted by: Wellcome Sanger Institute
Study: Viridans_Streptococci___A_genera_l__approach_to_surveillance
show Abstracthide Abstract
This project will allow the establishment of a solid baseline population structure of major and minor sequence clusters (as a proxy for speciation) within the Viridans streptococci and, in combination with existing sequence datasets from the pneumococcus, will form a solid basis for initial ‘speciation’ and fine scale clustering within lineages. Data will be provided through cGPS within a web application (www.wgsa.net) allowing the interrogation of metadata in a genomic context and forming a solid resource for the public health community
Sample: 3755STDY6172788
SAMEA104151680 • ERS1810698 • All experiments • All runs
Library:
Name: DN490184F:H10
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 3.4M spots, 845.1M bases, 294.3Mb
Run# of Spots# of BasesSizePublished
ERR27891133,380,340845.1M294.3Mb2018-09-13

ID:
6335486

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