|
Status |
Public on Nov 27, 2012 |
Title |
402198_preB |
Sample type |
genomic |
|
|
Channel 1 |
Source name |
preB, MspI representation of genomic DNA
|
Organism |
Homo sapiens |
Characteristics |
pathology: normal preB cells cytogenetics: NA immunophenotype: Pre-B site (pb: peripheral blood; BM: bone marrow): BM age: NA gender: NA white blood count (wbc, 10^9/l): NA %blasts: NA imatinib: NA overall_survival (days): NA code_os (dead_1): NA hyperdiploid: NA cd25: NA cd25(pos >=5%,_neg_<5%): NA
|
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 priming with 9-mers pre-labeled with either Cy3 or Cy5 according to manufacturer's instructions using the NimbleGen Dual-Color DNA Labeling Kit (cat # 06370381001)
|
|
|
Channel 2 |
Source name |
preB, HpaII representation of genomic DNA
|
Organism |
Homo sapiens |
Characteristics |
pathology: normal preB cells cytogenetics: NA immunophenotype: Pre-B site (pb: peripheral blood; BM: bone marrow): BM age: NA gender: NA white blood count (wbc, 10^9/l): NA %blasts: NA imatinib: NA overall_survival (days): NA code_os (dead_1): NA hyperdiploid: NA cd25: NA cd25(pos >=5%,_neg_<5%): NA
|
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 priming with 9-mers pre-labeled with either Cy3 or Cy5 according to manufacturer's instructions using the NimbleGen Dual-Color DNA Labeling Kit (cat # 06370381001)
|
|
|
|
Hybridization protocol |
See Roche NimbleGen website for the detailed manufacturers protocol.
|
Scan protocol |
Scanning was performed using NimbleGen MS 200 scanner
|
Description |
HELP DNA methylation array for normal preB cells from healthy bone marrows Sample name: Donor_B
|
Data processing |
Raw data (.pair) files generated using NimbleScan software. Signal intensities at each HpaII amplifiable fragment were calculated as a robust (20% trimmed) mean of their component probe-level signal intensities (as described in Khulan et al. Genome Research 2006). 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 considered as “failed” probes and marked as NA values. After QC processing for each array, a median normalization was performed on each array by subtracting the median log-ratio (HpaII/MspI) of that array (resulting in median log-ratio of 0 for each array).
|
|
|
Submission date |
Jan 09, 2012 |
Last update date |
Nov 27, 2012 |
Contact name |
Huimin Geng |
E-mail(s) |
huimin.geng@ucsf.edu
|
Organization name |
UCSF
|
Department |
Department of Laboratory Medicine
|
Street address |
513 Parnassus Ave., MSB S-1480
|
City |
San Francisco |
State/province |
CA |
ZIP/Postal code |
94143 |
Country |
USA |
|
|
Platform ID |
GPL6604 |
Series (2) |
GSE34937 |
Integrative Epigenomic Analysis Identifies Biomarkers and Therapeutic Targets in Adult B-Acute Lymphoblastic Leukemia [methylation profiling] |
GSE34941 |
Integrative Epigenomic Analysis Identifies Biomarkers and Therapeutic Targets in Adult B-Acute Lymphoblastic Leukemia |
|