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ERX2648574: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 7.1M spots, 1.8G bases, 624.2Mb downloads

Design: Illumina sequencing of library DN483412F:B6, constructed from sample accession ERS1646424 for study accession ERP011197. This is part of an Illumina multiplexed sequencing run (22538_2). This submission includes reads tagged with the sequence TGTATGCG.
Submitted by: SC (The Wellcome Trust 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: 3755STDY6172364
SAMEA103957256 • ERS1646424 • All experiments • All runs
Library:
Name: DN483412F:B6
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 7.1M spots, 1.8G bases, 624.2Mb
Run# of Spots# of BasesSizePublished
ERR26320807,083,1031.8G624.2Mb2018-07-04

ID:
5868120

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