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Sample GSM1679299 Query DataSets for GSM1679299
Status Public on May 11, 2015
Title dgcr8-/-_RNAseq
Sample type SRA
 
Source name mESCs
Organism Mus musculus
Characteristics cell type: dgcr8-/- mESCs
strain: V6.5
Growth protocol Mouse ESCs (V6.5, Dgcr8-/- and Dicer-/-) were cultured in DMEM with ESGRO (1000 units/mL), supplemented with 15% (v/v) FBS and antibiotics
Extracted molecule total RNA
Extraction protocol total RNAs were extracted using Trizol reagent
200 ng polyA(+) RNA isolated as described above was used for mRNA-seq. Sample preparation was with the TruSeq Stranded mRNA Sample Prep Kits (Illumina).10ug total RNAs was used for small RNA libraries preparaion fellowing small RNA Sample Prep Kits (Illumina)
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina MiSeq
 
Data processing bowtie softare is used to map reads to mRNA with two mismatches permitted, and self-developed perl scripts were used to coculate the reads of each genes
For small RNA sequencing, after removal of the adaptor sequences, bowtie software was used to mapping the small RNAs into mature miRNA sequences (miRBase).
Genome_build: mm9
Supplementary_files_format_and_content: RNAseq.txt provided a matrix table, which contained five columns including the gene's name, cDNA's name, reads number in WT, DGCR8 and Dicer samples; small RNA seq.txt provided the reads number for each miRNAs.
 
Submission date May 08, 2015
Last update date May 15, 2019
Contact name Peng Du
E-mail(s) Peng.Du@childrens.harvard.edu
Organization name Boston Children’s Hospital, Harvard Medical School
Lab Richard Gregory
Street address 1 Blackfan Circle
City Boston
State/province MA
ZIP/Postal code 02115
Country USA
 
Platform ID GPL16417
Series (1)
GSE68699 A biogenesis step upstream of Microprocessor controls miR-17~92 expression
Relations
BioSample SAMN03649544
SRA SRX1022480

Supplementary data files not provided
SRA Run SelectorHelp
Raw data are available in SRA
Processed data are available on Series record

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