NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4061304 Query DataSets for GSM4061304
Status Public on Feb 29, 2020
Title WT, ISO treated, replicate 1
Sample type SRA
 
Source name Blastocysts
Organism Mus musculus
Characteristics genotype: WT
treatment: Treated with 200 microM ISO for 6 hrs
cell type: Blastocysts
strain: C57BL/6
Treatment protocol Cells from the treatment group were treated with 200 µM Isoproterenol (Sigma, I2760) for 6 hrs before extracting RNA.
Growth protocol Cells were grown in 35mm dishes in DMEM (Fisher, 11-995-073) supplemented with 15% fetal bovine serum (Hyclone), penicillin/streptomycin (Fisher, 15-140-148), Glutamax (Fisher, 35-050-061), NEAA (Fisher, 11-140-050) and β-mercaptoethanol (Sigma, M3148) at 37 degree celcius in a 5% CO2 atmosphere.
Extracted molecule total RNA
Extraction protocol Total RNA was extracted using RNeasy Micro kit (Qiagen, 74004) according to manufacturer's specifications. Quality of RNA was assesed using Agilent 2100 Bioanalyzer (NANO).
500 ng of total RNA were used to prepare cDNA library using TruSeq Stranded mRNA Library Prep Kit (Illumina Inc., San Diego, CA, USA) with PolyA selection. The quality of libraries were assessed with Agilent 2200 TapeStation system.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
 
Description wtiso_1
Data processing Basecalling was performed using illumina's bcl2fastq (v1.8.4).
fastq_screen (v0.5.2) was used to quality check fastq reads for contamination by mapping against multiple genomes.
Trimmomatic (v0.36) was used to trim adapters and low quality bases.
STAR aligner (v2.6.0a) was used to align/map processed reads with reference genome.
Quantification of mapped reads were carried out using featureCounts from Subread package (v1.6.3)
Genome_build: mm10 from UCSC
Supplementary_files_format_and_content: countsPerMillion_filt_TMMnorm.txt is a tab-delimited text file which contains abundance mesurement of genes across the samples. The abundance is in the form of number of reads of genes which are filtered for lowly expressed genes using 'filterByExpr' function from R/Biconductor's EdgeR package and further normalized using Trimmed Mean Value (TMM) method -- to account for composition bias -- before converting them into counts per million to account for the library size difference among samples. The columns represent sample names and rows official gene symbols (NCBI).
 
Submission date Sep 05, 2019
Last update date Feb 29, 2020
Contact name Sandipkumar Darji
E-mail(s) sdarji@nki.rfmh.org
Organization name Nathan Kline Institute for Psychiatric Research
Department Center for Dementia Research
Street address 140 Old Orangeburg Rd, Bldg 39
City Orangeburg
State/province NY
ZIP/Postal code 10962
Country USA
 
Platform ID GPL17021
Series (1)
GSE136894 β2-adrenergic agonists rescue lysosome acidification and function in PSEN1 deficiency by reversing defective ER to lysosome delivery of ClC-7
Relations
BioSample SAMN12697732
SRA SRX6804084

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

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap