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ERX2656111: Illumina HiSeq 4000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 4000) run: 98.8M spots, 29.6G bases, 11.6Gb downloads

Design: Illumina sequencing of library DN522100K:A2, constructed from sample accession SAMEA4872132 for study accession ERP107342. This is part of an Illumina multiplexed sequencing run (25832_8). This submission includes reads tagged with the sequence GATCAG.
Submitted by: SC (The Wellcome Trust Sanger Institute)
Study: Sanger_VGP_RNAseq
show Abstracthide Abstract
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:
SAMEA4872132 • ERS2711098 • All experiments • All runs
Library:
Name: DN522100K:A2
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Construction protocol: RNA-seq dUTP prokaryotic
Runs: 1 run, 98.8M spots, 29.6G bases, 11.6Gb
Run# of Spots# of BasesSizePublished
ERR263961798,796,30929.6G11.6Gb2018-07-04

ID:
5870844

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