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ERX5970117: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 65.5M spots, 19.8G bases, 6Gb downloads

Design: Illumina sequencing of library DN589386E:C6, constructed from sample accession ERS3757565 for study accession ERP119445. This is part of an Illumina multiplexed sequencing run (31798_3). This submission includes reads tagged with the sequence GTTTGTTT.
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_RD8092200
SAMEA5787425 • ERS3757565 • All experiments • All runs
Library:
Name: DN589386E:C6
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: RNA PolyA
Runs: 1 run, 65.5M spots, 19.8G bases, 6Gb
Run# of Spots# of BasesSizePublished
ERR633844065,492,78719.8G6Gb2021-09-26

ID:
16386328

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