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ERX5970112: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 71.7M spots, 21.7G bases, 6.6Gb downloads

Design: Illumina sequencing of library DN589386E:F5, constructed from sample accession ERS3757561 for study accession ERP119445. This is part of an Illumina multiplexed sequencing run (31798_3). This submission includes reads tagged with the sequence TCCGGATT.
Submitted by: Wellcome Sanger Institute
Study: Transcriptome_data_for_Sanger_25_genomes_project
show Abstracthide Abstract
The study will produce transcriptomic data to be used in support of the annotation of 25 novel reference genomes representing a cross section of UK biodiversity.
Sample: DTOL_RD8092195
SAMEA5787421 • ERS3757561 • All experiments • All runs
Library:
Name: DN589386E:F5
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: RNA PolyA
Runs: 1 run, 71.7M spots, 21.7G bases, 6.6Gb
Run# of Spots# of BasesSizePublished
ERR633843571,690,00821.7G6.6Gb2021-09-26

ID:
16386323

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