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Sample GSM1848930 Query DataSets for GSM1848930
Status Public on Oct 15, 2015
Title Ute_PCP3
Sample type SRA
 
Source name Vestibular epithelium
Organism Mus musculus
Characteristics purification: Enzymatic/mechanical
c1 ifc #: IFC 2 Tube Control
gfp (i): N/A
tdtomato (i): N/A
classifications: Utricular epithelium bulk population
Treatment protocol All cells are untreated.
Growth protocol All cells used were from acute isolations from postnatal day 1 mice that carry transgenic alleles to fluorescently mark the supporting cells and hair cells of the inner ear.
Extracted molecule polyA RNA
Extraction protocol Following dissociation of tissue into a single-cell suspension, target cells were enriched by purification as described, cells were lysed, polyA RNA reverse-transcribed, and cDNA amplified using SMARTer ultra-low input cDNA synthesis (Clontech) on the C1 microfluidics platform (Fluidigm).
cDNA libraries were prepared for sequencing using Nextera XT tagmentation and 96-barcode indexing (Illumina). Barcoded samples were pooled, cleaned with Agencourt AMPure XP magnetic bead isolation (Beckman Coulter).
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 1000
 
Description 100-200 cell bulk population
Data processing Basecalling and sample demultiplexing by Illumina HAS 0.9
We prepared a Bowtie2_2.2.3 index from the NCBI whole genome mm10 reference transcriptome using default rsem1.2.19 parameters
Paired-end reads were aligned to transcriptome using rsem1.2.19 command rsem-calculate-expression -p 16 --calc-pme --calc-ci --ci-memory 20000 --bowtie2 --bowtie-chunkmbs 512 --no-bam-output --time --paired-end --forward-prob 0.5 --estimate-rspd *R1_001.fastq *R2_001.fastq /ReferenceLocation ./OutputLocation 2>./*.Log.txt 1>./*.Console.txt
Genome_build: NCBI GRCm38 (mm10)
Supplementary_files_format_and_content: Tab-delimited text file with the estimated expression (TPM) for each gene for each Sample as calculated by RSEM1.2.19. Tab-delmited text file with the estimated count for each gene for each Sample as calculated by RSEM1.2.19.
 
Submission date Aug 12, 2015
Last update date May 15, 2019
Contact name Michael C Kelly
E-mail(s) michael.kelly3@nih.gov
Organization name NCI
Department Center for Cancer Research
Lab Single Cell Analysis Facility
Street address 41 Center Drive
City Bethesda
State/province MD
ZIP/Postal code 20894
Country USA
 
Platform ID GPL15103
Series (1)
GSE71982 Single-cell RNA-Seq resolves cellular complexity in sensory organs from the neonatal inner ear
Relations
BioSample SAMN03983063
SRA SRX1142775

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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