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ERX4492754: Illumina HiSeq 4000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 4000) run: 79.3M spots, 23.8G bases, 8.8Gb downloads

Design: Illumina sequencing of library DN548878S:H10, constructed from sample accession SAMEA5574024 for study accession ERP107342. This is part of an Illumina multiplexed sequencing run (27847_7). This submission includes reads tagged with the sequence CTATGTGA.
Submitted by: Wellcome 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:
SAMEA5574024 • ERS5189251 • All experiments • All runs
Library:
Name: DN548878S:H10
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: RNA PolyA
Runs: 1 run, 79.3M spots, 23.8G bases, 8.8Gb
Run# of Spots# of BasesSizePublished
ERR455667579,285,05823.8G8.8Gb2020-09-02

ID:
11768472

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