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Status |
Public on Feb 28, 2022 |
Title |
H3K4me3_ChIP_NPC_WT_rep2 |
Sample type |
SRA |
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Source name |
neural precursor cells
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Organism |
Mus musculus |
Characteristics |
cell type: E14 mouse neural precursor cell chip antibody: H3K4me3 (Millipore, 04-745)
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Growth protocol |
Cells were grown in DMEM supplemented with 100 U/mL penicillin, 100 mg/mL streptomycin, 15% KnockOut Serum Replacement (ThermoFisher, 10828028), Glutamax (Gibco, 35050), 0.1 mM non-essential amino acid, 0.1mM beta-mercaptoethanol, and 500 U/ml LIF at 37°C and 5% CO2
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Extracted molecule |
genomic DNA |
Extraction protocol |
ChIP and input library preparation were carried out as described in ENCODE experiments (“Ren Lab ENCODE Chromatin Immunoprecipitation Protocol” in https://www.encodeproject.org/documents/) ChIP-seq library sequencing procedures were carried out as previously described according to Illumina HiSeq4000 or HiSeq2500 protocols (Illumina, San Diego, CA).
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 4000 |
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Data processing |
fastq: Illumina's HiSeq Control Software Each fastq file was mapped to mouse genom (mm10) with BWA -aln (Li and Durbin, 2009) and PCR duplicates were removed using Picard MarkDuplicate. The bigWig files were created using deepTools (Ramírez et al., 2016). Genome_build: mm10 Supplementary_files_format_and_content: The processed files (bigWig) were created using deepTools (Ramírez et al., 2016).
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Submission date |
Nov 05, 2020 |
Last update date |
Feb 28, 2022 |
Contact name |
Bing Ren |
Organization name |
University of California, San Diego School of Medicine
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Street address |
9500 Gilman Dr., CMM-East, Admin Area/Rm 2071
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City |
La Jolla |
State/province |
CA |
ZIP/Postal code |
92093 |
Country |
USA |
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Platform ID |
GPL21103 |
Series (2) |
GSE160890 |
KMT2C/KMT2D (MLL3/MLL4) Histone Methyltranferase Activity Dependent Chromatin Organization at Enhancers during Embryonic Stem Cell Differentiation [ChIP-seq] |
GSE160892 |
Mll3/Mll4 catalytic activity is necessary for de novo enhancer-promoter contacts during embryonic stem cell differentiation |
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Relations |
BioSample |
SAMN16675192 |
SRA |
SRX9443492 |
Supplementary data files not provided |
SRA Run Selector |
Raw data are available in SRA |
Processed data are available on Series record |
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