Illumina HiSeq 4000 paired end sequencing - SRA

ERX4524701: Illumina HiSeq 4000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 4000) run: 32.8M spots, 1.6G bases, 566.8Mb downloads

Design: Illumina sequencing of library DN618945D:B2, constructed from sample accession ERS4144571 for study accession ERP107342. This is part of an Illumina multiplexed sequencing run (33769_8). This submission includes reads tagged with the sequence ATTCCT.

Submitted by: Wellcome Sanger Institute

Study: Sanger_VGP_RNAseq

PRJEB25429 • ERP107342 • All experiments • All runs

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The Vertebrate Genomes Project aims to provide annotated reference genome sequences for all vertebrate species. The initial phase is targeting one species per order, although additional species may be sequenced from some orders. This study contains RNAseq data from both Ilumina and Pacific Biosciences platforms to support transcript and gene annotation of reference genomes obtained at the Sanger Institute for the Vertebrate Genomes Project. RNA extracts will be obtained from diverse tissues, with specific sources specified in the individual sample metadata.

Sample: VGPRNA8550532

SAMEA6378482 • ERS4144571 • All experiments • All runs

Organism: Notothenia coriiceps

Library:

Name: DN618945D:B2

Instrument: Illumina HiSeq 4000

Strategy: RNA-Seq

Source: TRANSCRIPTOMIC

Selection: PolyA

Layout: PAIRED

Construction protocol: Small RNA (miRNA)

Runs: 1 run, 32.8M spots, 1.6G bases, 566.8Mb

Run	# of Spots	# of Bases	Size	Published
ERR4591039	32,760,239	1.6G	566.8Mb	2020-09-16

ID:: 11898435

SRA

Sequence Read Archive

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