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ERX3961546: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 502,204 spots, 251.1M bases, 125.1Mb downloads

Design: Illumina sequencing of library DN443490W:B3, constructed from sample accession ERS4332778 for study accession ERP005466. This is part of an Illumina multiplexed sequencing run (19961_2). This submission includes reads tagged with the sequence TTCTGTGT.
Submitted by: Wellcome Sanger Institute
Study: ICONIC
PRJEB6008 • ERP005466 • All experiments • All runs
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Details to follow
Sample: 3034STDY6355545
SAMEA6568443 • ERS4332778 • All experiments • All runs
Organism: HIV-1 unknown group
Library:
Name: DN443490W:B3
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 502,204 spots, 251.1M bases, 125.1Mb
Run# of Spots# of BasesSizePublished
ERR3953741502,204251.1M125.1Mb2020-02-28

ID:
10226287

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