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ERX2403187: Illumina MiSeq paired end sequencing
1 ILLUMINA (Illumina MiSeq) run: 515,302 spots, 154.6M bases, 86.2Mb downloads

Design: Illumina sequencing of library DN514783E:E1, constructed from sample accession ERS2112040 for study accession ERP014415. This is part of an Illumina multiplexed sequencing run (25177_1). This submission includes reads tagged with the sequence ACAGTG.
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: 0007232v
SAMEA104500756 • ERS2112040 • All experiments • All runs
Library:
Name: DN514783E:E1
Instrument: Illumina MiSeq
Strategy: WGS
Source: VIRAL RNA
Selection: Inverse rRNA
Layout: PAIRED
Construction protocol: Ribozero RNA-seq (HMR)
Runs: 1 run, 515,302 spots, 154.6M bases, 86.2Mb
Run# of Spots# of BasesSizePublished
ERR2352311515,302154.6M86.2Mb2018-02-28

ID:
5171435

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