Illumina HiSeq 4000 paired end sequencing - SRA

ERX3161576: Illumina HiSeq 4000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 4000) run: 112M spots, 33.6G bases, 12.5Gb downloads

Design: Illumina sequencing of library DN540354J:C9, constructed from sample accession SAMEA5365133 for study accession ERP107342. This is part of an Illumina multiplexed sequencing run (27898_1). This submission includes reads tagged with the sequence TGTCAGCT.

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:

SAMEA5365133 • ERS3246197 • All experiments • All runs

Organism: Chelmon rostratus

Library:

Name: DN540354J:C9

Instrument: Illumina HiSeq 4000

Strategy: RNA-Seq

Source: TRANSCRIPTOMIC

Selection: PolyA

Layout: PAIRED

Construction protocol: RNA PolyA

Runs: 1 run, 112M spots, 33.6G bases, 12.5Gb

Run	# of Spots	# of Bases	Size	Published
ERR3132345	111,978,828	33.6G	12.5Gb	2019-02-08

ID:: 7241466

SRA

Sequence Read Archive

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