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Status |
Public on Mar 14, 2018 |
Title |
H3K4me1 Ngn3-low #2 |
Sample type |
SRA |
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Source name |
Pancreas
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Organism |
Mus musculus |
Characteristics |
embryonic day: E13.5 cell type: dorsal pancreas; Ngn3-low chip antibody: H3K4me1 (Millipore, 07-436)
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Extracted molecule |
genomic DNA |
Extraction protocol |
Low-cell-number ChIP-seq followed the method described by Brind'Amour et al. We used approximately 1.5 × 10e4 cells per ChIP with 1 ng antibodies of H3K4me3 (Abcam, ab8580), H3K27me3 (Millipore, 07-449), H3K4me1 (Millipore, 07-436), H3K27ac (Active motif, 39133), respectively. Library preparation was conducted with “Ultra DNA Library Prep Kit for Illumina” (NEB. E7370).
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Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
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Description |
H3K4me1_Ngn3-low.bdg.gz
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Data processing |
The sequencing reads were aligned to the Mus musculus genome (mm10) using bowtie2 (v2.2.5) with default parameters, and we only retained reads with a mapping quality ≥ 30 for subsequent analyses. PCR duplicate reads were removed using samtools (v1.3.1) with the commands “samtools sort in_bam | samtools rmdup -s - out_bam”. Reads of two biological replicates were pooled. Tag density was calculated and stored in the bedGraph format using Homer with the parameters “makeUCSCfile out_dir –o out.bdg –name sample_name -color track_color –fragLength 150 –avg -fsize 1e20”. genome build: mm10 processed data files format and content: bedGraph files were generated using Homer (v4.7.2); Scores represent read count per bp per 1 × 10e7 reads.
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Submission date |
Jul 12, 2016 |
Last update date |
May 15, 2019 |
Contact name |
Cheng-ran Xu |
Organization name |
Peking University
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Department |
School of Basic Medical Sciences
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Street address |
NO.5 YIHEYUAN ROAD HAIDIAN DISTRICT, BEIJING, P.R.CHINA
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City |
Beijing |
State/province |
- |
ZIP/Postal code |
100871 |
Country |
China |
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Platform ID |
GPL17021 |
Series (1) |
GSE84324 |
Dynamics of chromatin marks and the role of JMJD3 during pancreatic endocrine cell fate commitment |
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Relations |
BioSample |
SAMN05385882 |
SRA |
SRX1941082 |
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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