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Status |
Public on Nov 02, 2015 |
Title |
Sham_rep2 |
Sample type |
SRA |
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Source name |
nervous system
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Organism |
Rattus norvegicus |
Characteristics |
strain: Sprague-Dawley tissue: Dorsal root ganglion (DRG) treatment: Control, right side
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Extracted molecule |
total RNA |
Extraction protocol |
DRGs were removed, flash frozen on dry ice, andtotal RNA wasextracted using either Trizol reagent(Life Technologies) or RNeasy (Qiagen). Illumina TruSeq Stranded Total RNA with Ribo-zero Gold kits (RS-122-2301 was used with 1 ug of total RNA for the construction of sequencing libraries. RNA libraries were prepared for sequencing using standard Illumina protocols
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Library strategy |
RNA-Seq |
Library source |
transcriptomic |
Library selection |
cDNA |
Instrument model |
Illumina HiSeq 2500 |
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Description |
Control, right side
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Data processing |
Illumina Casava1.8 software used for basecalling. RNA-seq reads were aligned to the rn4 genome assembly using TopHat 2.0.9 with these parameters: -p 28 --b2-fast -G /UCSC/rn4/Annotation/Genes/genes.gtf --segment-length 20 Fragments Per Kilobase of exon per Megabase of library size (FPKM) and DE genes were calculated using cuffdiff v 2.1.1 with default parameters Genome_build: rn4 Supplementary_files_format_and_content: tab-delimited text files include RPKM values for each Sample ...
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Submission date |
Jul 02, 2014 |
Last update date |
May 15, 2019 |
Contact name |
matteo cesaroni |
Organization name |
Temple University
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Street address |
3307 N. Broad S, Rm 220, PAHB
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City |
Philadelphia |
State/province |
PA |
ZIP/Postal code |
19140 |
Country |
USA |
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Platform ID |
GPL18694 |
Series (1) |
GSE59043 |
G9a is essential for epigenetic silencing of K+ channel genes in acute-to-chronic pain transition |
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Relations |
BioSample |
SAMN02900657 |
SRA |
SRX644928 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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