HiSeq X Ten paired end sequencing - SRA

ERX3341615: HiSeq X Ten paired end sequencing
1 ILLUMINA (Illumina HiSeq X Ten) run: 91.4M spots, 27.6G bases, 11.9Gb downloads

Design: Illumina sequencing of library DN518444E:H1, constructed from sample accession SAMEA994732 for study accession ERP024552. This is part of an Illumina multiplexed sequencing run (25555_7). This submission includes reads tagged with the sequence CCAAGATG.

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:

SAMEA994732 • ERS3378290 • All experiments • All runs

Organism: Salmo trutta

Library:

Name: DN518444E:H1

Instrument: Illumina HiSeq X Ten

Strategy: WGS

Source: GENOMIC

Selection: RANDOM

Layout: PAIRED

Construction protocol: Chromium genome

Runs: 1 run, 91.4M spots, 27.6G bases, 11.9Gb

Run	# of Spots	# of Bases	Size	Published
ERR3316105	91,410,596	27.6G	11.9Gb	2019-05-09

ID:: 7812526

SRA

Sequence Read Archive

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