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ERX2403191: Illumina MiSeq paired end sequencing
1 ILLUMINA (Illumina MiSeq) run: 841,041 spots, 252.3M bases, 128.9Mb downloads

Design: Illumina sequencing of library DN514783E:A2, constructed from sample accession ERS2112044 for study accession ERP014415. This is part of an Illumina multiplexed sequencing run (25177_1). This submission includes reads tagged with the sequence GATCAG.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Sequencing_extracted_nucleic_acid_from_the_National_Collection_of_Pathogenic_Viruses
show Abstracthide Abstract
This project aims to sequence the genomes of RNA viruses in the National Collection of Pathogenic Viruses (NCPV) run by Public Health England. The NCPV preserves well-characterised, authenticated human pathogenic viruses in a secure facility, and supplies the agents or nucleic acids derived from them to the scientific community. The genomes sequenced within this project will be a valuable additional resource that will also be made available to the scientific community.
Sample: 0012037v
SAMEA104500760 • ERS2112044 • All experiments • All runs
Library:
Name: DN514783E:A2
Instrument: Illumina MiSeq
Strategy: WGS
Source: VIRAL RNA
Selection: Inverse rRNA
Layout: PAIRED
Construction protocol: Ribozero RNA-seq (HMR)
Runs: 1 run, 841,041 spots, 252.3M bases, 128.9Mb
Run# of Spots# of BasesSizePublished
ERR2352315841,041252.3M128.9Mb2018-02-28

ID:
5171439

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