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Sample GSM988216 Query DataSets for GSM988216
Status Public on Dec 31, 2013
Title CG-SH gDNA
Sample type SRA
 
Source name acute myeloid leukemia
Organism Homo sapiens
Characteristics cell line: CG-SH
Treatment protocol Cells were grown in exponential phase before 1x10^7 cells were collected and placed into either DNAzol or Trizol in order to extract gDNA or RNA respectively
Growth protocol Cells were cultured in IMDM medium with 10% FBS, penicillin (100 U/ml) and streptomycin (100 µg/ml) supplemented with cytokines (human stem cell factor (H-SCF) (100 ng/ml), interleukin 3 (IL-3) (20 ng/ml), granulocyte colony-stimulating factor (G-CSF) (20 ng/ml)
Extracted molecule genomic DNA
Extraction protocol gDNA was extracted from DNAzol (Invitrogen) according to manufacturers protocol. gDNA was used to created paired-end libraries using Illumina Truseq V3 kit according to manufacturers protocol.
 
Library strategy OTHER
Library source genomic
Library selection other
Instrument model Illumina HiSeq 2000
 
Data processing Illumina Casava1.7 software used for basecalling.
Eland2 was used (through Casava 1.7) for mapping to the human reference genome
Variants were called usign Samtools with a quality filter of 20 and a minimum number of reads equal or greater than 3
Genome Build: hg19
supplementary files format and content: Sequence variants in BCF format
 
Submission date Aug 17, 2012
Last update date May 15, 2019
Contact name Brian Wilhelm
E-mail(s) brian.wilhelm@umontreal.ca
Organization name University of Montreal
Street address 2950 Chemin Polytechnique
City Montreal
ZIP/Postal code H1J 3R4
Country Canada
 
Platform ID GPL11154
Series (1)
GSE40199 Whole Genome sequencing of a normal karyotype AML cell line
Relations
SRA SRX179256
BioSample SAMN01120801

Supplementary file Size Download File type/resource
GSM988216_build_cgsh.raw.bcf.gz 114.8 Mb (ftp)(http) BCF
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

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