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ERX5970110: Illumina NovaSeq 6000 paired end sequencing
1 ILLUMINA (Illumina NovaSeq 6000) run: 58.2M spots, 17.6G bases, 5.3Gb downloads

Design: Illumina sequencing of library DN589386E:D5, constructed from sample accession ERS3757560 for study accession ERP119445. This is part of an Illumina multiplexed sequencing run (31798_3). This submission includes reads tagged with the sequence GTGCTCGT.
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_RD8092193
SAMEA5787420 • ERS3757560 • All experiments • All runs
Library:
Name: DN589386E:D5
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: RNA PolyA
Runs: 1 run, 58.2M spots, 17.6G bases, 5.3Gb
Run# of Spots# of BasesSizePublished
ERR633843358,180,46817.6G5.3Gb2021-09-26

ID:
16386321

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