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Sample GSM7777992 Query DataSets for GSM7777992
Status Public on Apr 30, 2024
Title CHD053-20
Sample type genomic
 
Source name Case#5_t(8;21)
Organism Homo sapiens
Characteristics cell type: Unsorted Bone Marrow Cells
Treatment protocol None
Growth protocol None
Extracted molecule genomic DNA
Extraction protocol DNA were extracted from bone marrow cells of patients using All Prep DNA/RNA Mini Kit (Qiagen). DNA quality and quantity was assessed using a Nanodrop Spectrophotometer, Bioanalyzer and/or Tapestation visualization (Agilent 2100 Bioanalyzer) and agarose gel electrophoresis
Label Biotin
Label protocol As per manufacturer (Affymetrix)
 
Hybridization protocol DNA was restriction digested, ligated, PCR amplified, fragmented, labeled and hybridized to each array according to the manufacturer's instructions
Scan protocol The Arrays were then washed using Affymetrix fluidics stations, and scanned using the Gene Chip Scanner 3000 7G
Description CHD053-20
Data processing Protocol was supported by Affymetrix GeneChip Command Console (AGCC) software. Analysis was performed through Affymetrix Chromosome Analysis 4.0 (ChAS) software with filters set at 200 Kb for Copy Number Alterations (CNAs) and 10 Mb for copy neutral Loss Of Heterozygosity (cnLOH). Our data refer to NetAffx Build 32.3 (hg19) database
 
Submission date Sep 13, 2023
Last update date Apr 30, 2024
Contact name Cristina Mecucci
E-mail(s) cristina.mecucci@unipg.it
Phone +39 075 5783808
Organization name University of Perugia
Department Department of Medicine, Hematology and Bone Marrow Transplantation Unit
Lab Laboratory of Cytogenetics and Molecular Genetics
Street address Piazzale Menghini n.9
City Perugia
ZIP/Postal code 06132
Country Italy
 
Platform ID GPL16131
Series (2)
GSE243055 A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias [Copy number analysis]
GSE243056 A novel t(X;21) (p11.4;q22.12) translocation adds to the role of BCOR and RUNX1 in Myelodysplastic Syndromes/Acute Myeloid Leukemias

Data table header descriptions
ID_REF
VALUE Genotype Call (SNP call): AA, AB, BB, NC, and NoCall; 'Signal' = Summarized signal
WEIGHTED LOG2 RATIO
SMOOTH SIGNAL

Data table
ID_REF VALUE WEIGHTED LOG2 RATIO SMOOTH SIGNAL
C-7SARK -0.295955 -0.045409 2.149344
C-4WYLN 0.106253 0.058991 2.149044
C-3BFNY 0.147923 -0.024068 2.148355
C-7ONNE 0.111289 0.079999 2.148443
C-6HYCN 0.274609 0.163602 2.148370
C-7SCGC 0.332364 0.266999 2.148233
C-7RZQQ 0.252294 0.178915 2.148352
C-7RZWZ 0.031530 0.281286 2.148242
C-7SEBI -0.029618 -0.082308 2.148643
C-7RZIL -0.054558 0.018672 2.147238
C-4NQTX -0.185470 -0.076432 2.145113
C-7SDKW 0.152364 0.022785 2.145098
S-3WRNV nan nan nan
C-7RXVK -0.073833 -0.097461 2.144839
C-4LHKS 0.142926 -0.000365 2.144380
C-7RWHE -0.191279 -0.103012 2.143847
C-7SBEJ -0.087006 -0.008356 2.143606
C-7RYJO -0.180550 0.079292 2.143450
C-7SEGS 0.225118 0.171259 2.143129
C-4LLXK 0.095949 0.057880 2.143712

Total number of rows: 2749693

Table truncated, full table size 96028 Kbytes.




Supplementary file Size Download File type/resource
GSM7777992_CHD053-20_CytoScanHD_Array.CEL.gz 31.7 Mb (ftp)(http) CEL
GSM7777992_CHD053-20_CytoScanHD_Array.na33.cyhd.cychp.gz 95.3 Mb (ftp)(http) CYCHP

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