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ERX2666260: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 1.2M spots, 303.7M bases, 97.4Mb downloads

Design: Illumina sequencing of library DN444872N:B3, constructed from sample accession ERS1106585 for study accession ERP014540. This is part of an Illumina multiplexed sequencing run (19944_5). This submission includes reads tagged with the sequence TTCTGTGT.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: GAS_Vaccinology__Capturing_Global_Vaccine_Antigen_Diversity
show Abstracthide Abstract
This project consists of a two-phase action plan designed to validate the overall aims of the GAS vaccinology programme as well as generating publishable units from scientifically robust comparisons. Apart from vaccine antigen design, this programme of sequencing will support targeted analyses of specific disease associations and global transmission patterns of prominent sequence types- all ongoing sequencing based research foci that Sanger (Mark Davies) is currently analysing.
Sample: 2004V1230P
SAMEA3919451 • ERS1106585 • All experiments • All runs
Library:
Name: DN444872N:B3
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 1.2M spots, 303.7M bases, 97.4Mb
Run# of Spots# of BasesSizePublished
ERR26497701,214,925303.7M97.4Mb2018-07-04

ID:
5872582

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