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Sample GSM3334225 Query DataSets for GSM3334225
Status Public on Oct 11, 2018
Title UB_RNASeq
Sample type SRA
Source name Ureteric epithelium
Organism Mus musculus
Characteristics tissue: Ureteric epithelium
cell type: Ureteric epithelium (manually dissected)
strain: C57BL/6
genotype: wild type
age: E11.5
chip antibody: n/a
Extracted molecule total RNA
Extraction protocol Libraries were prepared using SMARTer Stranded Total RNA Sample Prep Kit - HI Mammalian (Clontech Laboratories)
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2500
Description Cuffdiff_MM_UB_transcript_FPKM.tabular
Data processing For ChIP-seq analysis, the replicate was concatenated and mapped using Bowtie2 at default setting.
ChIP-seq peaks were called using MACS14 against the input control data. The parameter set used in MACS14 was as follows: H3K4me3 (Band width 300, Pvalue cutoff 1e-05, the nearby regions to calculate dynamic lambda 1000-10000) and H3K27me3 (Band width 2900, Pvalue cutoff 1e-04 (mES and MM(Cited1)) or 1e-03 (UB), the nearby regions to calculate dynamic lambda 1000-20000).
Peaks were annotated with overlapping genes using AnnotateGenomicRegions (
For RNA-seq analysis, all sequencing reads were mapped using Tophat at default setting.
Aligned RNA-seq reads were further analyzed using Cufflinks, Cuffmerge, and Cuffdiff
Genome_build: mm10
Supplementary_files_format_and_content: ChIP-seq: BED files with called peaks on sample records and peak annotation files on series record.
RNA-seq: text file with FPKM
Submission date Aug 15, 2018
Last update date Oct 11, 2018
Contact name Masaki Nishikawa
Organization name UCLA / VA
Lab Yanagawa
Street address 16111 Plummer st
City North Hills
State/province CA
ZIP/Postal code 91343
Country USA
Platform ID GPL17021
Series (1)
GSE118607 Comprehensive analysis of chromatin signature and transcriptome in nephron progenitor cells
BioSample SAMN09839547
SRA SRX4557400

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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