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ERX11137532: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 1.3M spots, 396.4M bases, 24Mb downloads

Design: Illumina sequencing of library DN924906D:C1, constructed from sample accession ERS12273114 for study accession ERP136353. This is part of an Illumina multiplexed sequencing run (45404_1). This submission includes reads tagged with the sequence GTTAACGT.
Submitted by: Wellcome Sanger Institute
Study: GBS__Kawempe
PRJEB51700 • ERP136353 • All experiments • All runs
show Abstracthide Abstract
This project will allow us to generate evidence on: • prevalence of GBS serotypes and genotypes in women and babies at birth in this setting • transmission of GBS between mothers, and from mother to baby • association of GBS genetics with carriage and/or disease • nosocomial colonisation
Sample: Streptococcus agalactiae
SAMEA110174301 • ERS12273114 • All experiments • All runs
Organism: Streptococcus agalactiae
Library:
Name: DN924906D:C1
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: pWGS-384
Runs: 1 run, 1.3M spots, 396.4M bases, 24Mb
Run# of Spots# of BasesSizePublished
ERR117367521,312,676396.4M24Mb2023-09-01

ID:
29104204

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