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ERX3961513: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 466,791 spots, 233.4M bases, 119.8Mb downloads

Design: Illumina sequencing of library DN443491A:F9, constructed from sample accession ERS4332915 for study accession ERP005466. This is part of an Illumina multiplexed sequencing run (19961_1). This submission includes reads tagged with the sequence GATCTCTT.
Submitted by: Wellcome Sanger Institute
Study: ICONIC
Sample: 3034STDY6355701
SAMEA6568580 • ERS4332915 • All experiments • All runs
Library:
Name: DN443491A:F9
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 466,791 spots, 233.4M bases, 119.8Mb
Run# of Spots# of BasesSizePublished
ERR3953708466,791233.4M119.8Mb2020-02-28

ID:
10226254

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