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ERX3419800: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 3.7M spots, 745.2M bases, 384.7Mb downloads

Design: Illumina sequencing of library DN483659D:D4, constructed from sample accession ERS1751291 for study accession ERP022712. This is part of an Illumina multiplexed sequencing run (22866_2). This submission includes reads tagged with the sequence TACAGGAT.
Submitted by: Wellcome Sanger Institute
Study: Characterising_the_molecular_basis_of_treatment_failure_in_Neisseria_gonorrhoeae_infection_
show Abstracthide Abstract
Neisseria gonorrhoea represents an important cause of vaginal bacteriosis. As part of a recent clinical trial evaluating different treatment regimens, a small number of patients appeared to fail treatment, and remained gonorrhoea positive post-treatment. This project will use direct sequencing approaches from residual NAAT samples to study the genotype of reoccurring strains to discriminate between relapse and reinfection, as well as investigating the microevolutionary changes associated with ongoing vaginal colonisation under selective drug pressure. This data is part of a pre-publication release. For information on the proper use of pre-publication data shared by the Wellcome Trust Sanger Institute (including details of any publication moratoria), please see http://www.sanger.ac.uk/datasharing/
Sample: 4721STDY6851381
SAMEA104087398 • ERS1751291 • All experiments • All runs
Library:
Name: DN483659D:D4
Instrument: Illumina HiSeq 2500
Strategy: WXS
Source: GENOMIC
Selection: Hybrid Selection
Layout: PAIRED
Construction protocol: Agilent Pulldown
Runs: 1 run, 3.7M spots, 745.2M bases, 384.7Mb
Run# of Spots# of BasesSizePublished
ERR33959373,725,861745.2M384.7Mb2023-03-09

ID:
26903396

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