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Sample GSM1648491 Query DataSets for GSM1648491
Status Public on Jun 19, 2015
Title shRad21_RNAseq
Sample type SRA
 
Source name immortalized fibroblast
Organism Mus musculus
Characteristics strain: CAST/Ei x 129/Sv/Jae
cell type: Xi GFP tail-tip fibroblast
antibody: none
genetic manipulation: Stable shRNA knockdown of Rad21
Treatment protocol Cells were treated with 0.3 uM azacytidine and 0.3 uM etoposide for 3 days
Growth protocol Cells were cultured in regular fibroblast medium (1% Pen/Strep, high-glucose DMEM+GlutaMAX) with 10% FBS
Extracted molecule total RNA
Extraction protocol ChIP-seq:Cells were crosslinked with 1% formaldeyde for 10 min, then nuclei were isolated and lysed. Chromatin was sheared by sonication to a size of ~200-400 bp. Cleared lysates were precleared for 1 hour, then 10% saved as input, and lysates were incubated with Dynabeads Protein G pre-bound with the antibody of choice. After stringent washes, ChIP DNA was eluted from beads, and together with input chromtain was reverse-crosslinked with proteinase K. DNA was purified by phenol/chloroform extraction and ethanol precipitation. Hi-C: Hi-C experiments were conducted using HindIII according to the method described in Lieberman-Aiden, E. et al. Comprehensive mapping of long-range interactions reveals folding principles of the human genome. Science 326, 289-93 (2009). RNA-seq: Xi-TgGFP TTFs (68-5-11) with the stable knock down of candidates were treated with 5’-azacytidine and etoposide at 0.3 M each for 3 days. Strand specific RNA-seq, the library preparation, deep sequencing, and data analysis was followed as described in J. T. Kung et al., Locus-specific targeting to the X chromosome revealed by the RNA interactome of CTCF. Molecular cell 57, 361-375 (2015). All libraries were sequenced with Illumina Hiseq 2000 or 2500 using 50 cycles to obtain paired end reads.
ChIP-seq: Libraries were constructed using the NEBNext ChIP-seq Library Preparation Kit with no modifications to the protocol. We used 16 cycles during the PCR step. Hi-C: Sequencing libraries were constructed according to the method described in Lieberman-Aiden, E. et al. Comprehensive mapping of long-range interactions reveals folding principles of the human genome. Science 326, 289-93 (2009). RNA-seq: Total RNA was harvested using trizol extraction, and ribosomal RNA was removed using RiboMinus. Strand-specific libraries were generated by performing reverse transcription with Superscript III, followed by second-strand synthesis using the NEBNext second-strand synthesis module supplemented with dUTP, and then libraries were generated using the NEBNext ChIP-seq Library Preparation Kit.
 
Library strategy RNA-Seq
Library source transcriptomic
Library selection cDNA
Instrument model Illumina HiSeq 2000
 
Description s4_mus/ reads
Data processing ChIP-seq: Reads were aligned separately to the mus/129 and cas genomes using novoalign with default parameters for paired-end alignment, the coordinates of these alignments were then converted to mm9 coordinates with custom scripts. Following alignment, coverage files were generated for the composite set of reads (comp), as well as allelic reads that aligned better to mus (mus) or cas (cas) using custom perl scripts, SAMtools and bedtools to extract and sort allelic reads, remove duplicates and generate coverage files. The coverage files presented in the paper and in this archive are fpm normalized. Peaks were called using macs2 with default settings. Hi-C: The individual ends of the read-pairs were aligned to the mus and cas reference genomes separately using novoalign with default parameters for single-end alignments, and the quality score of the alignment was used to determine whether each end could be assigned to either the mus or the cas haplotype. The single-end alignments were merged into a HiCsummary file using custom scripts to determine whether a given read-pair could be assigned to the mus or cas haplotype and to pair up the two ends of the read-pair. RNA-seq: To determine the allelic origin of each sequencing read from the hybrid cells, reads were first depleted of adaptors dimers and PCR duplicates, followed by the alignment to custom mus/129 and cas genomes to separate mus and cas reads. Once completed, reads were then mapped back to reference mm9 genome using Tophat v2.0.10 (-g 1 --no-coverage-search --read-edit-dist 3 --read-mismatches 3 --read-gap-length 3 --b2-very-sensitive --mate-inner-dist 50 --mate-std-dev 50 --library-type fr-firststrand). Following alignment, gene expression levels within each library were quantified using Homer v4.7 (rna mm9 -count genes -strand + -noadj -condenseGenes) and the normalized differential expression analyses across samples were performed by using EdgeR.
Genome_build: mm9
Supplementary_files_format_and_content: ChIP-seq: bigWig (bw) files for all reads (.comp), regardless of whether they are allele-specific or not, cas-specific (.cas) and mus-specific (.mus). All bigWig files are fpm-normalized, but not input normalized or smoothed. Hi-C: data is present in a Hi-C summary file, where each line corresponds to the coordinates of the the two end-pairs in the alignment. RNA-seq: aligned reads used for analysis are present in .bed files. Reads aligning to the + strand of the genome are in the "+" files and reads aligning to the - strand are in the - files. As for the ChIP-seq, reads are broken down into comp, cas and mus sets. Supplementary files included in this series consist of an excel file containing .fpkm values and the results of the differential expression analysis using edgeR for all RNA-seq experiments.
 
Submission date Apr 01, 2015
Last update date May 15, 2019
Contact name John Edward Froberg
E-mail(s) jfroberg@fas.harvard.edu
Phone 8479770174
Organization name Harvard University
Department Stem Cell & Regenerative Biology
Lab Macklis Lab
Street address 7 Divinity Avenue
City Cambridge
State/province MA
ZIP/Postal code 02138
Country USA
 
Platform ID GPL13112
Series (1)
GSE67516 A comprehensive Xist interactome reveals cohesin repulsion and an RNA-directed chromosome conformation
Relations
Reanalyzed by GSE94418
BioSample SAMN03456800
SRA SRX976740

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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