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SRX20977296: GSM7593190: MII_rep_4; Sus scrofa; RNA-Seq
1 ILLUMINA (NextSeq 500) run: 35.9M spots, 2.7G bases, 1.1Gb downloads

External Id: GSM7593190_r1
Submitted by: Obstetrics & Gynaecology, The University of Adelaide
Study: RNA-sequencing of pig oocyte throughout meiotic maturation
show Abstracthide Abstract
Oocyte maturation refers to oocytes at the germinal vesicle stage progressing into metaphase II (MII) stage of development. Even though numerous studies have shown key genes and potential important signalling cascades, which drive the GV to MII transition, a system-wide analysis of underlying differences at gene level and especially at transcript level between the two developmental stages of the oocyte is still lacking. For this, we profiled and analysed RNA from pig oocytes across meiotic maturation (GV, MII and damaged, n=15). We detected 22,516 genes for each sample across meiotic maturation. Principal Component analysis of the data clustered the samples in three stages of development (GV, MII and damaged). Differential expression of genes between the three stages will then be used to delineate the pathways which are up-/down-regulated during these developmental stages. Besides, differential transcript usage will be used to identify the difference of oocytes at distinct developmental stages at isoform level, which might be ignored by traditional differential gene expression analysis. Overall design: Pig oocyte mRNA profiles from three developmental stages, GV (germinal vesicle, n=5), MII (metaphase II, n=5) and 'damaged' (oocytes without visible polar body after in vitro maturation/IVM, n = 5)
Sample: MII_rep_4
SAMN36401939 • SRS18253329 • All experiments • All runs
Organism: Sus scrofa
Library:
Name: GSM7593190
Instrument: NextSeq 500
Strategy: RNA-Seq
Source: TRANSCRIPTOMIC
Selection: cDNA
Layout: SINGLE
Construction protocol: The SMART-Seq® HT kit (Takara Bio Inc., Shiga, Japan) was used for cDNA generation according to the manufacturer's instructions using 13 PCR cycles across a total of 15 samples. cDNAs were then converted to sequencing libraries using the Illumina DNA Prep kit (Illumina, San Diego, USA) according to the manufacturer's instructions with 8 PCR cycles for the final amplification. An equimolar pool of libraries was sequenced by single-end RNA sequencing (1 x 75bp) on an Illumina Nextseq 500 at the South Australian Genomics Centre (SAGC; Adelaide, SA).
Runs: 1 run, 35.9M spots, 2.7G bases, 1.1Gb
Run# of Spots# of BasesSizePublished
SRR2523077035,899,3722.7G1.1Gb2024-07-11

ID:
28411081

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