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ERX3961498: Illumina HiSeq 2500 paired end sequencing
1 ILLUMINA (Illumina HiSeq 2500) run: 684,096 spots, 342M bases, 173.8Mb downloads

Design: Illumina sequencing of library DN443491A:G7, constructed from sample accession ERS4332900 for study accession ERP005466. This is part of an Illumina multiplexed sequencing run (19961_1). This submission includes reads tagged with the sequence TTCGCACC.
Submitted by: Wellcome Sanger Institute
Study: ICONIC
Sample: 3034STDY6355685
SAMEA6568565 • ERS4332900 • All experiments • All runs
Library:
Name: DN443491A:G7
Instrument: Illumina HiSeq 2500
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Standard
Runs: 1 run, 684,096 spots, 342M bases, 173.8Mb
Run# of Spots# of BasesSizePublished
ERR3953693684,096342M173.8Mb2020-02-28

ID:
10226239

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