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Sample GSM1362187 Query DataSets for GSM1362187
Status Public on Mar 24, 2015
Title R0_5.10_earleaf
Sample type genomic
 
Channel 1
Source name CL5.10_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 CL5.10_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 CL5.10
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 0.0871080849466152
CHR10FS000075774 0.921372394381111
CHR10FS000163060 0.615190487763592
CHR10FS000163660 -0.88753757469576
CHR10FS000188003 0.319852817121261
CHR10FS000193884 0.40759138333618
CHR10FS000270288 -0.0751616364638578
CHR10FS000275537 0.529814661995838
CHR10FS000275737 -0.171065943061507
CHR10FS000276542 0.914452150957258
CHR10FS000276742 0.338571420388968
CHR10FS000276942 0.57114930649786
CHR10FS000277142 0.435138584349825
CHR10FS000279446 0.683383977851503
CHR10FS000299425 0.253402975160049
CHR10FS000299625 0.508679046483995
CHR10FS000299921 0.744970442117396
CHR10FS000300429 0.0370002012719911
CHR10FS000300629 -0.631900214780522
CHR10FS000300829 -1.2762760223466

Total number of rows: 1400988

Table truncated, full table size 47068 Kbytes.




Supplementary file Size Download File type/resource
GSM1362187_5-10_532_grid.pair.gz 26.3 Mb (ftp)(http) PAIR
GSM1362187_5-10_635_grid.pair.gz 26.3 Mb (ftp)(http) PAIR
Processed data included within Sample table

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