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ERX4524654: Illumina HiSeq 4000 paired end sequencing
1 ILLUMINA (Illumina HiSeq 4000) run: 45.6M spots, 2.3G bases, 766.4Mb downloads

Design: Illumina sequencing of library DN618935B:F2, constructed from sample accession ERS4144523 for study accession ERP107342. This is part of an Illumina multiplexed sequencing run (33769_2). This submission includes reads tagged with the sequence AGTTCC.
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: VGPRNA8550427
SAMEA6378434 • ERS4144523 • All experiments • All runs
Library:
Name: DN618935B:F2
Instrument: Illumina HiSeq 4000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: PolyA
Layout: PAIRED
Construction protocol: Small RNA (miRNA)
Runs: 1 run, 45.6M spots, 2.3G bases, 766.4Mb
Run# of Spots# of BasesSizePublished
ERR459099245,613,7662.3G766.4Mb2020-09-16

ID:
11898298

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