HiSeq X Ten paired end sequencing - SRA

ERX3341693: HiSeq X Ten paired end sequencing
1 ILLUMINA (Illumina HiSeq X Ten) run: 113.1M spots, 34.1G bases, 13.8Gb downloads

Design: Illumina sequencing of library DN539765J:D1, constructed from sample accession SAMEA5248726 for study accession ERP024552. This is part of an Illumina multiplexed sequencing run (26963_3). This submission includes reads tagged with the sequence CGCCATCG.

Submitted by: Wellcome Sanger Institute

Study: 25_Genomes_for_25_Years_of_Genomics

PRJEB22206 • ERP024552 • All experiments • All runs

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The Study will produce 25 novel reference genomes representing a cross section of UK biodiversity. These will be sequenced to a depth of 50x using long-read and 50x using short-read (Illumina) technologies, complemented with 10x Chromium sequencing.

Sample:

SAMEA5248726 • ERS3567203 • All experiments • All runs

Organism: Vespa velutina

Library:

Name: DN539765J:D1

Instrument: Illumina HiSeq X Ten

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Chromium genome

Runs: 1 run, 113.1M spots, 34.1G bases, 13.8Gb

Run	# of Spots	# of Bases	Size	Published
ERR3316183	113,057,795	34.1G	13.8Gb	2019-05-09

ID:: 7812596

SRA

Sequence Read Archive

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