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Sample GSM615050 Query DataSets for GSM615050
Status Public on May 17, 2011
Title 1345518-13455531 - H3K4me2_C24_III_IP vs H3K4me2_C24_III_INPUT
Sample type genomic
 
Channel 1
Source name H3K4me2_C24_III_INPUT
Organism Arabidopsis thaliana
Characteristics strain: c24
age: 10 day
tissue: seedling
sample type: input DNA
Treatment protocol no treatment
Growth protocol seedling - 10 days in liquid MS 0.5X at 22 degrees C. Cool white light at 100 uEm-2s-1, 16 hour photoperiod.
Extracted molecule genomic DNA
Extraction protocol C24_III:50ug.
Label Cy5
Label protocol labelling Cy3 and Cy5 direct, amplification=yes, DNA .
 
Channel 2
Source name H3K4me2_C24_III_IP
Organism Arabidopsis thaliana
Characteristics strain: c24
age: 10 day
tissue: seedling
antibody: H3K4me2
antibody manufacturer: upstate
antibody catalog #: 07-030
Treatment protocol no treatment
Growth protocol seedling - 10 days in liquid MS 0.5X at 22 degrees C. Cool white light at 100 uEm-2s-1, 16 hour photoperiod.
Extracted molecule genomic DNA
Extraction protocol C24_III:50ug. antibody: H3K4me2 (upstate_07-030);
Label Cy3
Label protocol labelling Cy3 and Cy5 direct, amplification=yes, DNA .
 
 
Hybridization protocol H3K4me2_C24_III_INPUT Cy5 / H3K4me2_C24_III_IP Cy3 : 80pmol.
Scan protocol GenePix Pro 3.0, Cy3:pmt voltage 532nm,550V,laser power 100%, Cy5:635nm,pmt voltage 600V,laser power 100%
Description arabidopsis thaliana (c24) - age: 10day dev.stage (Boyes et al. Plant Cell 2001):seedling
Arabidopsis thaliana accessions (Col-0, C24 and Cvi) and their hybrid were used to investigate the dynamics of the epigenome after intraspecific hybridization between
Data processing Data were normalized as ChIP-chip data in Turck e al.(2007). This method is based on the properties of dye-swaps to remove technical biases. To be specific, let Yij be the signal of the sample labeled with the dye j on the array i. Given that the second array is a technical replicate of the first one, the distribution of Y21 (respectively Y22) should be close to that of Y12 (respectively Y11). In practice, the relationship between Y21 and Y12 is linear but it is not the identity function. The parameters of the two linear models are estimated by Y21=a+bY12+N(0,sigma2) and Y22=c+dY11+N(0,sigma2),and these estimates are used to define the normalized IP and INPUT values of the second array relative to the first one: Y21=(Y21-a)/b and Y22=(Y22-c)/d.For each sample and for each tile, the values of the two arrays of the dye-swap are then averaged.To analyze data, we use ChIPmix, a method proposed by Martin-Magniette et al.(2008) that we have adapted to study several biological replicates simultaneously. The method investigates the relationship between IP and Input by a mixture model of regressions. For a probe, available observation are the two measurements IP and INPUT for the two biological replicates. These latter are assumed to be independent by definition. The (unknown) status of a probe is characterized through a label Z which is 1 if the probe is enriched and 0 if it is normal (not enriched).
 
Submission date Nov 01, 2010
Last update date May 17, 2011
Contact name François ROUDIER
E-mail(s) francois.roudier@ens-lyon.fr
Organization name Ecole Normale Supérieure de Lyon
Department Biologie
Lab RDP
Street address 46 Allée d'Italie
City Lyon
ZIP/Postal code 69364
Country France
 
Platform ID GPL10772
Series (2)
GSE24836 Analysis of epigenomic changes in hybrids Arabidopsis thaliana Col-0, C24 and Cvi accessions
GSE25049 h3k4me2_c24_chr4-Analysis of epigenomic changes in hybrids Arabidopsis thaliana Col-0, C24 and Cvi accessions

Data table header descriptions
ID_REF ID
VALUE Normalized log ratio base 2 IP/INPUT (INPUT=reference)
Intensity_cy5 Normalized intensity of Ch1(Cy5) = INPUT
Intensity_cy3 Normalized intensity of Ch2(Cy3) = IP
STATUS (0/1) 1 if the FDR.BH < 0.01 and 0 otherwise
FDR.BH The false discovery rate (FDR) were controlled at the 1% level using a Benjamini and Hochberg correction probability

Data table
ID_REF VALUE Intensity_cy5 Intensity_cy3 STATUS FDR.BH
BAR
BT
C037
C041
C042
C043
C065
C100
C150
C160
C227
C228
GFP
GLOBIN
GUS
HPH
LUC
M001
M005
M006

Total number of rows: 21800

Table truncated, full table size 1187 Kbytes.




Supplementary file Size Download File type/resource
GSM615050_1345518-13455531.gpr.gz 1.7 Mb (ftp)(http) GPR
Processed data included within Sample table

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