Illumina NovaSeq 6000 paired end sequencing - SRA

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

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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

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 Bases	Size	Published
ERR11736752	1,312,676	396.4M	24Mb	2023-09-01

ID:: 29104204

SRA

Sequence Read Archive

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