|
Status |
Public on Mar 30, 2012 |
Title |
input DNA for TCF7 |
Sample type |
SRA |
|
|
Source name |
EML cells
|
Organism |
Mus musculus |
Characteristics |
sequence type: Illumina; single-end;35bp reads antibody: none cell type: Lin-SCA+CD34+ cells
|
Growth protocol |
EML cell culture was maintained in expansion medium (IMDB, 20% heat inactivated horse serum, 100 ng/ml SCF [PeproTech])
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Cell lysates were clarified from sonicated nuclei and transcription factor-DNA complexes were isolated with antibody. DNA sequencing followed the instructions of the mRNA-Sequencing Sample Prep Kit (Illumina).
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina Genome Analyzer |
|
|
Description |
input DNA
|
Data processing |
Alignment: Sequence reads were obtained and mapped to the mouse mm9 genomes using the Illumina Genome Analyzer Pipeline. All reads mapping with two or fewer mismatches were retained.
|
|
|
Submission date |
Aug 04, 2011 |
Last update date |
May 15, 2019 |
Contact name |
Jiaqian Wu |
E-mail(s) |
jiaqian2009.wu@gmail.com
|
Organization name |
Stanford University
|
Street address |
1501 California Avenue
|
City |
PALO ALTO |
ZIP/Postal code |
94306 |
Country |
USA |
|
|
Platform ID |
GPL9185 |
Series (1) |
GSE31221 |
TCF7 is a key regulator of the switch of self-renewal and differentiation in a multipotential hematopoietic cell line |
|
Relations |
SRA |
SRX092475 |
BioSample |
SAMN00710419 |