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Sample GSM1362186 Query DataSets for GSM1362186
Status Public on Mar 24, 2015
Title R0_4.10_earleaf
Sample type genomic
 
Channel 1
Source name CL4.10_input, R0
Organism Zea mays
Characteristics line: A188
tissue: first ear leaf
replication: 1
sample type: input
Treatment protocol Genomic DNAs were sonicated, amplified, and fluorophore-labeled.
Growth protocol Maize plants (A188 genotype) were grown under controlled conditions in a greenhouse at the University of Wisconsin-Madison (Madison, WI) with a light cycle of 15 hours lights on and 9 hours lights off each day. Maize plants were watered daily as needed.
Extracted molecule genomic DNA
Extraction protocol Callus used for DNA extraction was collected from each cell line prior to plating onto R1 media after six months of culturing. The uppermost flag leaf of R0 plants and the 3rd leaf of R1 plants were harvested for DNA extraction to conduct meDIP-Chip profiling (Zymo Research DNA methylation IP kit D5101). All tissues were immediately flash-frozen in liquid N2. DNA was isolated using a modified CTAB method.
Label Cy3
Label protocol Amplified input and methylated DNA samples were labeled (3 x 1ug per reaction), hybridized to the array and washed according to the array manufacturer's protocol. Input DNAs were labeled using Cy3 and the immunoprecipitated methylated DNAs (IP) were labeled with Cy5.
 
Channel 2
Source name CL4.10_IP, R0
Organism Zea mays
Characteristics line: A188
tissue: first ear leaf
replication: 1
sample type: methylated DNA (IP pulldown)
Treatment protocol Genomic DNAs were sonicated, methylated DNAs were isolated, amplified, and fluorophore-labeled.
Growth protocol Maize plants (A188 genotype) were grown under controlled conditions in a greenhouse at the University of Wisconsin-Madison (Madison, WI) with a light cycle of 15 hours lights on and 9 hours lights off each day. Maize plants were watered daily as needed.
Extracted molecule genomic DNA
Extraction protocol Callus used for DNA extraction was collected from each cell line prior to plating onto R1 media after six months of culturing. The uppermost flag leaf of R0 plants and the 3rd leaf of R1 plants were harvested for DNA extraction to conduct meDIP-Chip profiling (Zymo Research DNA methylation IP kit D5101). All tissues were immediately flash-frozen in liquid N2. DNA was isolated using a modified CTAB method.
Label Cy5
Label protocol Amplified input and methylated DNA samples were labeled (3 x 1ug per reaction), hybridized to the array and washed according to the array manufacturer's protocol. Input DNAs were labeled using Cy3 and the immunoprecipitated methylated DNAs (IP) were labeled with Cy5.
 
 
Hybridization protocol 24-34ug of labeled DNAs (input DNA, IP DNA) were hybridized to the arrays according to the array manufacturer's protocol (42°C, 16-20hrs).
Scan protocol Arrays were scanned according to the NimbleScan CGH User Guide protocol, which specifies parameters for the MS2000 Scanner (NimbleGen) used to collect data.
Description CL4.10
Data processing Images were aligned and quantified using NimbleScan software (Roche NimbleGen) which produced .pair reports of raw data.
Pair files that were exported from NimbleScan were imported into the Bioconductor statistical environment (Gentleman et al., 2004). Signal was first loess normalized within each array to minimize space effect and then quantile normalized across arrays to minimize batch effect. This was done through the Ringo Bioconductor package in R for the management and normalization of NimbleGen microarray data.
 
Submission date Apr 02, 2014
Last update date Mar 24, 2015
Contact name Steve R Eichten
E-mail(s) [email protected]
Organization name University of Minnesota
Department Plant Biology
Lab Springer Lab
Street address 1445 Gortner Ave
City St. Paul
State/province MN
ZIP/Postal code 55108
Country USA
 
Platform ID GPL15621
Series (1)
GSE56479 Consistent and Heritable Alterations of DNA Methylation are Induced by Tissue Culture in Maize

Data table header descriptions
ID_REF
VALUE Normalized log2 ratio (IP/input)

Data table
ID_REF VALUE
CHR10FS000075407 0.145437707273796
CHR10FS000075774 0.115564963705972
CHR10FS000163060 0.349643531294102
CHR10FS000163660 0.233235489733518
CHR10FS000188003 0.183120242933629
CHR10FS000193884 0.652416148827065
CHR10FS000270288 0.574503754482831
CHR10FS000275537 0.194040964252631
CHR10FS000275737 0.316358532107229
CHR10FS000276542 0.545787026091333
CHR10FS000276742 0.305688587399131
CHR10FS000276942 -0.094532817521186
CHR10FS000277142 -0.0477542988452212
CHR10FS000279446 0.44279239277008
CHR10FS000299425 0.461913405525204
CHR10FS000299625 0.433321050526646
CHR10FS000299921 0.477121689496043
CHR10FS000300429 -0.57467831583672
CHR10FS000300629 -0.700772175846416
CHR10FS000300829 -1.14573391621961

Total number of rows: 1400988

Table truncated, full table size 47067 Kbytes.




Supplementary file Size Download File type/resource
GSM1362186_4-10_532_grid.pair.gz 26.4 Mb (ftp)(http) PAIR
GSM1362186_4-10_635_grid.pair.gz 26.3 Mb (ftp)(http) PAIR
Processed data included within Sample table

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