Illumina NovaSeq 6000 paired end sequencing - SRA

ERX11165652: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 1.7M spots, 503.6M bases, 33.7Mb downloads

Design: Illumina sequencing of library DN924909G:N23, constructed from sample accession ERS12273700 for study accession ERP136353. This is part of an Illumina multiplexed sequencing run (45433_1). This submission includes reads tagged with the sequence CCAGCATC.

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

SAMEA110174886 • ERS12273700 • All experiments • All runs

Organism: Streptococcus agalactiae

Library:

Name: DN924909G:N23

Instrument: Illumina NovaSeq 6000

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: pWGS-384

Runs: 1 run, 1.7M spots, 503.6M bases, 33.7Mb

Run	# of Spots	# of Bases	Size	Published
ERR11766816	1,667,489	503.6M	33.7Mb	2023-09-01

ID:: 29120860

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Sequence Read Archive

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