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SRX3174680: ControlR1
1 ILLUMINA (HiSeq X Ten) run: 61.9M spots, 18.6G bases, 7.7Gb downloads

Design: Total RNA was extracted from tissues using a TaKaRaMiniBEST PlantRNA Extraction Kit. During total RNA extraction, genomic DNA was removed by the DNase I treatment.Then RNA was analyzed either using a ND-8000spectrophotometer (NanodropTechnologies, Inc., Wilmington, DE, USA) after purification, by agarose gelelectrophoresis, or using a2100-Bioanalyzer(AgilentTechnologies, Santa Clara, CA, USA) to determine the RNA quantity. Those RNA samples with no smear seen on agarose gels, a 260/280 ratio above 2.0, and a RNA integrity number greater than 8.0 were used. For RNA-sequencing, RNA samples (three biological replicates per conditionand four plants per replicate) were then sent to Genergy Biotechnology Corporation (http://www.genenergy.cn/) for sequencing. Total RNA was first depleted of rRNA using the Ribo-Zero rRNA removal kit (Plant Leaf and Plant Seed/Root kits; Epicentre), namely, 1 μg of total RNA from root samples was used as input for rRNAremoval. Sequencing libraries were generated using the TruSeq RNA sample prep kit (Illumina). The libraries were sequenced as 151-bp paired-end reads using Illumina HiSeq X ten according to the manufacturer's instructions.
Submitted by: College of Life Sciences, Nanjing Agricultural University (College of Life Sciences, Nanjing Agricultural Uni)
Study: Oryza sativa Transcriptome under micronutrient deficiency in root.
show Abstracthide Abstract
Identify mirocronutrient deficiency dys-regulated genes using high-throughput RNA sequencing of rice roots under different mineral deficient growth conditions (Fe-, Zn-, Cu- or Mn-deficient).
Sample:
SAMN07627063 • SRS2504575 • All experiments • All runs
Library:
Name: Ribo-Zero rRNA removal
Instrument: HiSeq X Ten
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: other
Layout: PAIRED
Spot descriptor:
forward152  reverse

Runs: 1 run, 61.9M spots, 18.6G bases, 7.7Gb
Run# of Spots# of BasesSizePublished
SRR620038261,851,92418.6G7.7Gb2018-05-11

ID:
4476464

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