Illumina NovaSeq 6000 paired end sequencing - SRA

ERX11165658: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 1.2M spots, 364.5M bases, 21.5Mb downloads

Design: Illumina sequencing of library DN924909G:G24, constructed from sample accession ERS12273840 for study accession ERP136353. This is part of an Illumina multiplexed sequencing run (45433_1). This submission includes reads tagged with the sequence GCCTCTCG.

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

SAMEA110175026 • ERS12273840 • All experiments • All runs

Organism: Streptococcus agalactiae

Library:

Name: DN924909G:G24

Instrument: Illumina NovaSeq 6000

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: pWGS-384

Runs: 1 run, 1.2M spots, 364.5M bases, 21.5Mb

Run	# of Spots	# of Bases	Size	Published
ERR11766822	1,207,062	364.5M	21.5Mb	2023-09-01

ID:: 29120866

SRA

Sequence Read Archive

Result Filters

Send to:

Supplemental Content

Related information

Recent activity