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Sample GSM2402626 Query DataSets for GSM2402626
Status Public on Dec 01, 2021
Title shUHRF1_Rep2
Sample type SRA
 
Source name Embryonic Dorsal Root Ganglia_shUHRF1
Organism Mus musculus
Characteristics strain: CD-1
developmental stage: Embryonic day 13
tissue: Dorsal Root Ganglia
knockdown: shUHRF1
Treatment protocol Cells were either treated with shUHRF1 or shControl lentivirus as described
Extracted molecule total RNA
Extraction protocol Invitrogen PureLink RNA Minikit with on-column Dnase treatment
Ribo-Zero Gold rRNA depletion then Clontech SMARTer cDNA Synthesis kit
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Data processing Adapter ends were trimmed using FastQC
Reads were aligned to mm10 using STAR-align with default settings
Reads aligned to genes were counted using Htseq-counts with default settings
Differential expression was calculated using DESeq2
Genome_build: mm10
Supplementary_files_format_and_content: Text files include gene counts; XLSX File includes differential expression analysis from DESeq2
 
Submission date Nov 23, 2016
Last update date Dec 01, 2021
Contact name Valeria Cavalli
E-mail(s) [email protected]
Organization name Washington University in St. Louis
Department Anatomy and Neurobiology
Street address 660 S. Euclid Ave.
City Saint Louis
State/province Missouri
ZIP/Postal code 63110
Country USA
 
Platform ID GPL17021
Series (2)
GSE90476 miRNA-9 regulates axon regeneration through the transcriptional regulator REST and the epigenetic factor UHRF1 [RNA-seq]
GSE90477 Gene repression by DNA methylation promotes axon regeneration
Relations
BioSample SAMN06051252
SRA SRX2371087

Supplementary file Size Download File type/resource
GSM2402626_shUHRF1_Rep2.counts.txt.gz 195.3 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file
Processed data are available on Series record

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