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Sample GSM2616867 Query DataSets for GSM2616867
Status Public on Jul 12, 2017
Title DFL_E12_Inv_Island-IIVP
Sample type SRA
 
Source name Forelimb
Organism Mus musculus
Characteristics strain: C57Bl6CBAF1
age: E12.5
genotype: HOXDInv(TpSB1-Itga6)
Extracted molecule genomic DNA
Extraction protocol Micro-dissected proximal and distal segments of E12.5 limbs either from wild type or mutant embryos were dissected, dissociated with collagenase (Sigma Aldrich/Fluka) and filtered through a 35 micron mesh to isolate single cells. Cells were fixed with 2% formaldehyde for 10 min at room temperature and the reaction was quenched on ice with glycine. Cells were further lysed with 10 mM Tris pH 7.5, 10 mM NaCl, 5 mM MgCl2, 0.1 mM EGTA, 1x Protease inhibitor cocktail to isolate nuclei and stored at -80°C. Nuclei from pools of at least 8 distal or proximal limbs were digested with NlaIII (New England Biolabs) and ligated with T4 DNA ligase HC (Promega) in diluted conditions to promote intramolecular ligation. Sequences ligated to fragments of interest were digested again with DpnII (New England Biolabs), ligated with T4 DNA ligase HC (Promega) in diluted conditions.
These templates were amplified using Expand long template (Roche) and inversed PCR primers flanked with adaptors allowing multiplexing. Hoxd13_inverse_forward: AATGATACGGCGACCACCGAACACTCTTTCCCTACACGACGCTCTTCCGATCTAAAATCCTAGACCTGGTCAT, Hoxd13-inverse_reverse: CAAGCAGAAGACGGCATACGAGGCCGATGGTGCTGTATAG, Isl_II forward primer: GCATTCATCAAGCTGTGATTAGCA, Isl_II reverse primer: TCCCATAATATGTAGACTGTAGTGTTGC.
For sample 9 we used a series of four different barcoded primers for Hoxd13 forward such as barcode 1: AATGATACGGCGACCACCGAACACTCTTTCCCTACACGACGCTCTTCCGATCTATCGAAAAATCCTAGACCTGGTCATG; iHoxd13 forward: barcode 2: AATGATACGGCGACCACCGAACACTCTTTCCCTACACGACGCTCTTCCGATCTGACAAAAAATCCTAGACCTGGTCATG; iHoxd13 forward: barcode3: AATGATACGGCGACCACCGAACACTCTTTCCCTACACGACGCTCTTCCGATCTTGACAAAAATCCTAGACCTGGTCATG; and iHoxd13 forward: barcode4: AATGATACGGCGACCACCGAACACTCTTTCCCTACACGACGCTCTTCCGATCTGGTAAAAAATCCTAGACCTGGTCATG
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2500
 
Description Distal limb mouse E12.5_Isl-II_VP_Inv
Data processing De-multiplexing, mapping and 4C-analysis were performed through HTSstation (David et al, 2014 and http://htsstation.epfl.ch/). Reads were mapped to the mm10 (GRCm38) mouse genome assembly with bowtie version 0.12.7 (Langmead et al, 2009) with parameters “-n 2 --best -strata -m 5”. Genome coverage densities were calculated for each strand separately, then averaged and normalized by the total number of mapped reads (times 10^-7).
4C figures were made using smoothed/normalized data that were obtained by applying a running mean algorithm with a window size of eleven fragments and normalized to the same total intensity, such as to see only changes in contacts distribution and to minimize PCR complexity bias in each samples.
Genome_build: mm10
Supplementary_files_format_and_content: Smoothed/normalized data (bedGraph), one per viewpoint, per tissue
 
Submission date May 12, 2017
Last update date May 15, 2019
Contact name Pierre J Fabre
E-mail(s) fabre.pierre@gmail.com
Organization name EPFL
Department ISREC
Lab Laboratory of Developmental Genomics
Street address Station 19
City Lausanne
ZIP/Postal code CH-1015
Country Switzerland
 
Platform ID GPL17021
Series (2)
GSE98233 Large-scale genomic reorganizations of topological domains (TADs) at the HoxD locus
GSE98861 Large-scale genomic reorganizations of topological domains (TADs) at the HoxD locus (4C-Seq)
Relations
BioSample SAMN06952613
SRA SRX2804247

Supplementary file Size Download File type/resource
GSM2616867_DFL_E12_INV_Isl-II_VP.bedgraph.gz 907.7 Kb (ftp)(http) BEDGRAPH
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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