|
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 |