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SRX12419617: Sinaechinocyamus mai gut transcriptome
1 ILLUMINA (Illumina NovaSeq 6000) run: 64.4M spots, 13G bases, 3.8Gb downloads

Design: Tissue subsamples were chopped and preserved in RNAlater (Ambion) buffer solution for 1 day at 4C, followed by long-term storage at -80C until RNA extraction. Total RNA was extracted from 1.5 mm Triple-Pure High Impact Zirconium beads (Benchmark Scientific) in Trizol (Ambion) using Direct-zol RNA Miniprep Kit (Zymo Research) with in-column DNase I incubation. Total RNA concentration was estimated using Qubit RNA HS Assay Kit (Invitrogen), and quality assessed using either High Sensitivity RNA ScreenTape or RNA ScreenTape with an Agilent 4200 TapeStation. Mature mRNA was isolated from total RNA and libraries were prepared using KAPA mRNA HyperPrep Kit (KAPA Biosystems), targeting an insert size of approx. 500 base pairs, and using custom 10-nucleotide Illumina TruSeq style adapters. Post-amplification, DNA concentration was estimated using Qubit dsDNA BR Assay Kit (Invitrogen). Concentration, quality, and molecular weight distribution of libraries was assessed using Genomic DNA ScreenTape with an Agilent 4200 TapeStation. Ten libraries were sequenced on one lane of a multiplexed run using NovaSeq S4 platform with 100 bp paired-end reads at the IGM Genomics Center (University of California San Diego)
Submitted by: Yale University
Study: Phylotranscriptomics of Echinoidea
show Abstracthide Abstract
The projects involves the sequencing of transcriptomes from a sample of highly-divergent echinoid lineages in order to provide a basis for a phylogenomic classification of the group
Sample: Sinaechinocyamus mai transcriptome
SAMN21905103 • SRS10387195 • All experiments • All runs
Library:
Name: SMAI
Instrument: Illumina NovaSeq 6000
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: PAIRED
Runs: 1 run, 64.4M spots, 13G bases, 3.8Gb
Run# of Spots# of BasesSizePublished
SRR1613455764,447,58013G3.8Gb2022-06-30

ID:
16831088

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