HiSeq X Ten paired end sequencing - SRA

ERX3341607: HiSeq X Ten paired end sequencing
1 ILLUMINA (Illumina HiSeq X Ten) run: 83.1M spots, 25.1G bases, 10.4Gb downloads

Design: Illumina sequencing of library DN518444E:F1, constructed from sample accession SAMEA994721 for study accession ERP024552. This is part of an Illumina multiplexed sequencing run (25555_5). This submission includes reads tagged with the sequence TTCAGGTG.

Submitted by: Wellcome Sanger Institute

Study: 25_Genomes_for_25_Years_of_Genomics

PRJEB22206 • ERP024552 • All experiments • All runs

show Abstracthide Abstract

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:

SAMEA994721 • ERS3567218 • All experiments • All runs

Organism: Vespa velutina

Library:

Name: DN518444E:F1

Instrument: Illumina HiSeq X Ten

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Chromium genome

Runs: 1 run, 83.1M spots, 25.1G bases, 10.4Gb

Run	# of Spots	# of Bases	Size	Published
ERR3316097	83,116,403	25.1G	10.4Gb	2019-05-09

ID:: 7812518

SRA

Sequence Read Archive

Result Filters

Send to:

Supplemental Content

Related information

Recent activity