NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM464952 Query DataSets for GSM464952
Status Public on Jan 12, 2010
Title 6370
Sample type genomic
 
Channel 1
Source name AML blast cells
Organism Homo sapiens
Characteristics digestion: Msp1
age: 57
gender: female
fab: M1
cytogenetic_class: -9q
cytogenetic_risk: Intermediate
11q23: Neg
3q: Neg
7q: Neg
5q: Neg
t(15;17): Neg
t(8;21): Neg
inv(16): Neg
tri 8: Neg
t(6;9): Neg
t(9;22): Neg
complex: Neg
other: Pos
normal karyotype: Neg
flt3itd: Neg
flt3tkd: Neg
flt3itdortkd: Neg
npm1: Neg
npm1plusflt3itdplus: Neg
npm1plusflt3itdneg: Neg
flt3itdplusnpm1neg: Neg
nras: Neg
kras: Neg
cebpa: Neg
ckit_exon8_id: Neg
ckit_exon17_d816: Neg
Extracted molecule genomic DNA
Extraction protocol Representation of the genome generated by digestion with either MspI or HpaII and amplification by ligation-mediated PCR according to the HELP protocol (See B. Khulan, et al. Genome Res. 2006 Aug;16(8):1046-55)
Label Cy3
Label protocol Random 9-mers pre-labeled with either Cy3 or Cy5
 
Channel 2
Source name AML blast cells
Organism Homo sapiens
Characteristics digestion: HpaII
age: 57
gender: female
fab: M1
cytogenetic_class: -9q
cytogenetic_risk: Intermediate
11q23: Neg
3q: Neg
7q: Neg
5q: Neg
t(15;17): Neg
t(8;21): Neg
inv(16): Neg
tri 8: Neg
t(6;9): Neg
t(9;22): Neg
complex: Neg
other: Pos
normal karyotype: Neg
flt3itd: Neg
flt3tkd: Neg
flt3itdortkd: Neg
npm1: Neg
npm1plusflt3itdplus: Neg
npm1plusflt3itdneg: Neg
flt3itdplusnpm1neg: Neg
nras: Neg
kras: Neg
cebpa: Neg
ckit_exon8_id: Neg
ckit_exon17_d816: Neg
Extracted molecule genomic DNA
Extraction protocol Representation of the genome generated by digestion with either MspI or HpaII and amplification by ligation-mediated PCR according to the HELP protocol (See B. Khulan, et al. Genome Res. 2006 Aug;16(8):1046-55)
Label Cy5
Label protocol Random 9-mers pre-labeled with either Cy3 or Cy5
 
 
Hybridization protocol See Roche NimbleGen website and Selzer RR, Richmond TA, Pofahl NJ, Green RD, Eis PS, et al. (2005) Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH. Genes Chromosomes Cancer 44: 305-319. for details
Scan protocol Scanning was performed using a GenePix 4000B scanner (Axon Instruments) as previously described in Selzer RR, Richmond TA, Pofahl NJ, Green RD, Eis PS, et al. (2005) Analysis of chromosome breakpoints in neuroblastoma at sub-kilobase resolution using fine-tiling oligonucleotide array CGH. Genes Chromosomes Cancer 44: 305-319.
Description none
Data processing Signal intensities at each HpaII amplifiable fragment were calculated as a robust (25% trimmed) mean of their component probe-level signal intensities. Any fragments found within the level of background MspI signal intensity, measured as 2.5 mean-absolute-differences (MAD) above the median of random probe signals, were categorized as “failed.” These “failed” loci therefore represent the population of fragments that did not amplify by PCR, whatever the biological (e.g. genomic deletions and other sequence errors) or experimental cause. On the other hand, “Methylated” loci were so designated when the level of HpaII signal intensity was similarly indistinguishable from background. PCR-amplifying fragments (those not flagged as either “methylated” or “failed”) were normalized using an intra-array quantile approach wherein HpaII and MspI signals are aligned across density-dependent sliding windows of fragment size-sorted data (described in detail in Thompson et al, Bioinformatics 2008;24:1161-1167). After intra-array normalization each channel was centered by subtracting background noise (2.5 median absolute deviations from the median of the random probes’ log2 signal for that channel) from its log2-transformed signal intensities. The HpaII/MspI (unmethylated/reference) ratio was then determined for each probe set on array.
 
Submission date Oct 23, 2009
Last update date Jan 12, 2010
Contact name Maria Eugenia Figueroa
E-mail(s) mef162@miami.edu
Organization name University of Miiami
Department Human Genetics
Lab Maria Figueroa
Street address 1501 NW 10th Ave, BRB 709A, Locator code C227
City Miami
State/province FL
ZIP/Postal code 33136
Country USA
 
Platform ID GPL6604
Series (1)
GSE18700 Genome-wide DNA methylation profiling of Acute Myeloid Leukemia

Data table header descriptions
ID_REF
VALUE log2 Ratio (HpaII/MspI)

Data table
ID_REF VALUE
MSPI0406S00000183 -2.235300791
MSPI0406S00000238 -1.734795875
MSPI0406S00000239 -1.159245869
MSPI0406S00000300 2.299547817
MSPI0406S00000301 1.043327203
MSPI0406S00000321 1.706469006
MSPI0406S00000352 1.01355722
MSPI0406S00000353 2.832360955
MSPI0406S00000354 -0.045194428
MSPI0406S00000360 -1.119600381
MSPI0406S00000361 -0.73838565
MSPI0406S00000384 1.400107542
MSPI0406S00000385 3.086243929
MSPI0406S00000410 0.432082816
MSPI0406S00000433 0.368595385
MSPI0406S00000434 0.326373927
MSPI0406S00000435 0.308426153
MSPI0406S00000479 -1.946041784
MSPI0406S00000480 -1.697632159
MSPI0406S00000492 -1.373600886

Total number of rows: 25626

Table truncated, full table size 761 Kbytes.




Supplementary file Size Download File type/resource
GSM464952_199561_532.pair.gz 6.3 Mb (ftp)(http) PAIR
GSM464952_199561_635.pair.gz 6.1 Mb (ftp)(http) PAIR
Processed data included within Sample table

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap