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ERX11138273: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 1M spots, 315.4M bases, 19.1Mb downloads

Design: Illumina sequencing of library DN924914D:F11, constructed from sample accession ERS12274215 for study accession ERP136353. This is part of an Illumina multiplexed sequencing run (45420_1). This submission includes reads tagged with the sequence CCGAATAA.
Submitted by: Wellcome Sanger Institute
Study: GBS__Kawempe
PRJEB51700 • ERP136353 • All experiments • All runs
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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
SAMEA110175402 • ERS12274215 • All experiments • All runs
Organism: Streptococcus agalactiae
Library:
Name: DN924914D:F11
Instrument: Illumina NovaSeq 6000
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: pWGS-384
Runs: 1 run, 1M spots, 315.4M bases, 19.1Mb
Run# of Spots# of BasesSizePublished
ERR117374941,044,257315.4M19.1Mb2023-09-01

ID:
29104945

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