|
Status |
Public on Apr 03, 2013 |
Title |
H3K79me2_MLL-AF6 rep3 |
Sample type |
SRA |
|
|
Source name |
Leukemic bone marrow cells, primary
|
Organism |
Mus musculus |
Characteristics |
background strain: B6/129 (Taconic) chip antibody: H3K79me2 cell type: Leukemic bone marrow cells, primary disease state: MLL-AF6 positive leukemia chip antibody manufacturer: Abcam chip antibody cataolog #: Ab3594
|
Treatment protocol |
Frozen leukemia bone marrow cells were thawed using standard conditions and 1 million cells were used for fixing and subsequent ChIP seq steps.
|
Growth protocol |
Cells were not grown prior to the ChIP-seq
|
Extracted molecule |
genomic DNA |
Extraction protocol |
DNA was sheared from the fixed MLL-AF6 leukemia cells using sonication. Histone-DNA complexes enriched for H3K79me2 were isolated by immunoprecipitation with the Abcam anti-H3K79me2 specific antibody (Ab 3594) ChIP DNA libraries were made following the Illumina ChIP-seq library preparation kit.
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Description |
ChIP-Seq Multiplexing using Illumina adapters
|
Data processing |
Sequence reads were aligned to human genome assembly mm9 using BWA with default parameters. Wiggle files were generated using a using a custom pipeline. Genome_build: mm9 Supplementary_files_format_and_content: wig
|
|
|
Submission date |
Dec 20, 2012 |
Last update date |
May 15, 2019 |
Contact name |
Amit Sinha |
E-mail(s) |
amit.sinha@childrens.harvard.edu
|
Phone |
617-582-7579
|
Organization name |
Dana-Farber Cancer Institute
|
Department |
Pediatric Oncology
|
Lab |
Armstrong Lab
|
Street address |
44 Binney St
|
City |
Boston |
State/province |
MA |
ZIP/Postal code |
02135 |
Country |
USA |
|
|
Platform ID |
GPL13112 |
Series (2) |
GSE43062 |
Genome wide mapping of histone 3 lysine 79 dimethylation in MLL-AF6 murine leukemias |
GSE43069 |
MLL-AF6 leukemia |
|
Relations |
SRA |
SRX212166 |
BioSample |
SAMN01832294 |