Illumina MiSeq paired end sequencing - SRA

ERX2403208: Illumina MiSeq paired end sequencing
1 ILLUMINA (Illumina MiSeq) run: 548,885 spots, 164.7M bases, 79.5Mb downloads

Design: Illumina sequencing of library DN514784F:B1, constructed from sample accession ERS2111970 for study accession ERP014415. This is part of an Illumina multiplexed sequencing run (25178_1). This submission includes reads tagged with the sequence CGATGT.

Submitted by: SC (The Wellcome Trust Sanger Institute)

Study: Sequencing_extracted_nucleic_acid_from_the_National_Collection_of_Pathogenic_Viruses

PRJEB12890 • ERP014415 • All experiments • All runs

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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: 0201138v

SAMEA104500686 • ERS2111970 • All experiments • All runs

Organism: Coxsackievirus A9

Library:

Name: DN514784F:B1

Instrument: Illumina MiSeq

Strategy: WGS

Source: VIRAL RNA

Selection: Inverse rRNA

Layout: PAIRED

Construction protocol: Ribozero RNA-seq (HMR)

Runs: 1 run, 548,885 spots, 164.7M bases, 79.5Mb

Run	# of Spots	# of Bases	Size	Published
ERR2352332	548,885	164.7M	79.5Mb	2018-02-28

ID:: 5171456

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