NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM4852512 Query DataSets for GSM4852512
Status Public on Jun 06, 2021
Title Nanog bait 1_ESC_Rep1
Sample type SRA
 
Source name Embryonic stem cells
Organism Mus musculus
Characteristics cell type: Embryonic stem cells
cell culture: 2i-LIF grown
umi-4c bait: Nanog bait 1
Treatment protocol untreated
Growth protocol Mouse embryonic stem cells (ESC) were cultured in naïve (2i) conditions and neural stem cells were cultured in EGF/FGF media.
Extracted molecule genomic DNA
Extraction protocol cell were fixed and extracted nuclei were processed so to capture DNA fragments in close proximity.
Libraries were constructed according to the UMI-4C protocol. Please see methods section of manuscript for further information.
UMI-4C libraries were pooled and sequenced on a HiSeq 2500 platform.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Data processing Library strategy: UMI-4C
UMI-4C raw data were processed using the ‘umi4cPackage’ (v0.0.0.9000) pipeline from the Tanay Lab
To briefly summarize the pipeline
raw reads are parsed through the UMI-4C pipeline, those reads containing the bait and padding sequence are retained and demultiplexed if required
The retained reads are split based on a perfect match to the restriction enzyme sequence to create a segmented fastq file. The first 10 bases of read 2 are extracted and attached to the segments derived from each read pair. Segments are aligned to the mm10 genome using bowtie2.
UMI filtering is used to determine the number of molecules supporting each ligation event, this information is stored in an adj table
The resulting UMI-4C tracks are then imported into R where the molecule counts per ligated fragment can be visualized / interrogated
Genome_build: mm10
Supplementary_files_format_and_content: The final tracks after processing through the umi4cPackage pipeline, converted to a readable text file. Contains the number of molecules supporting each ligation event
 
Submission date Oct 25, 2020
Last update date Jun 06, 2021
Contact name Suzana Hadjur
E-mail(s) s.hadjur@ucl.ac.uk
Phone +44 7798957199
Organization name Ucl
Department Cancer biology
Lab Genome organization
Street address 72 Huntley street
City London
ZIP/Postal code Wc1e6bt
Country United Kingdom
 
Platform ID GPL17021
Series (2)
GSE160015 STAG proteins mediate heterochromatin organization to support translation and cell identity [UMI-4C]
GSE160390 PEZIC_STAG1_Pluripotency
Relations
BioSample SAMN16539303
SRA SRX9353372

Supplementary file Size Download File type/resource
GSM4852512_processed_Nanog_bait_1_ESC_Rep1.txt.gz 401.1 Kb (ftp)(http) TXT
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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