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SRX27092207: RNA-Seq of Crassostrea ariakensis
1 BGISEQ (BGISEQ-500) run: 23.9M spots, 6.9G bases, 3.5Gb downloads

Design: Total RNA was extracted using the TRIzol reagent (Invitrogen, CA, USA) accordingtothemanufacturers protocol. RNA purity and quantification were evaluated using the NanoDrop2000spectrophotometer (Thermo Scientific, USA). RNA integrity was assessed usingtheAgilent2100Bioanalyzer (Agilent Technologies, Santa Clara, CA, USA). Then the libraries were constructedusingVAHTS Universal V47 RNA_seq Library Prep Kit according to the manufacturers instructions. Thetranscriptome sequencing and analysis were conducted by OE Biotech Co., Ltd. (Shanghai, China).
Submitted by: Institute of Oceanology, Chinese Academy of Sciences
Study: Crassostrea ariakensis Transcriptome or Gene expression
show Abstracthide Abstract
We evaluated and compared the transcriptional profiles and lncRNAs profiles of eight tissues (gill [G], smooth muscle [SmM], striated muscle [StM], marginal mantle [MM], inside mantle [IM], heart, lip and hepatopancreas [HE]) in Suminoe oyster in response to hyper-/hypo-saline stresses.
Sample:
SAMN45853382 • SRS23551065 • All experiments • All runs
Library:
Name: S_20_3
Instrument: BGISEQ-500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 23.9M spots, 6.9G bases, 3.5Gb
Run# of Spots# of BasesSizePublished
SRR3172983123,863,8906.9G3.5Gb2024-12-16

ID:
36570034

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