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ERX3357032: HiSeq X Ten paired end sequencing
1 ILLUMINA (Illumina HiSeq X Ten) run: 125.3M spots, 35G bases, 15.5Gb downloads

Design: Illumina sequencing of library DN478356G:F1, constructed from sample accession SAMEA104026374 for study accession ERP021269. This is part of an Illumina multiplexed sequencing run (22150_1). This submission includes reads tagged with the sequence ACCCTCCT.
Submitted by: Wellcome Sanger Institute
Study: Vertebrate_Genome_Project_FISH
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Part of the Vertebrate Genome Project, fish study.
Sample:
SAMEA104026374 • ERS2227384 • All experiments • All runs
Library:
Name: DN478356G:F1
Instrument: Illumina HiSeq X Ten
Strategy: WGS
Source: GENOMIC
Selection: RANDOM
Layout: PAIRED
Construction protocol: Chromium genome
Runs: 1 run, 125.3M spots, 35G bases, 15.5Gb
Run# of Spots# of BasesSizePublished
ERR3332317125,276,75435G15.5Gb2019-05-21

ID:
7889504

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