|
Status |
Public on Jun 27, 2013 |
Title |
FANCD2_IP_UV treated |
Sample type |
SRA |
|
|
Source name |
FANCD2_IP_UV treated
|
Organism |
Homo sapiens |
Characteristics |
cell type: human cell lines (kidney, embryonic) antibody: FANCD2 cell line: 293T
|
Treatment protocol |
UV treatment (30J), harvest post 3hour after UV treatment
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Lysates were clarified from sonicated nuclei and histone-DNA complexes were isolated with antibody. Libraries were prepared according to Illumina's instructions accompanying the DNA Sample Kit (Part# 0801-0303).
|
|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2000 |
|
|
Data processing |
Briefly, we mapped the reads with Bowtie version 0.12.7 to hg19 using the parameters -n 1 (which restricts the number of missmatches allowed in the alignment seed region to 1) and -m 1 (which suppresses all alignments for a read if more than 1 alignment exists for that read in the genome). For each report we generated we first use a program called "makeTagDirectory.pl" to prepare the read data for analysis by HOMER (e.g., it normalizes and provides basic QC). Then we use a program called 'analyzeChIP-Seq.pl' in HOMER that automates the analysis by stringing the following functions (programs) together into a pipeline: Peak finding / Transcript detection / Feature identification (findPeaks) Genome_build: mm9 Supplementary_files_format_and_content: HOMER Peaks Text files
|
|
|
Submission date |
May 14, 2013 |
Last update date |
May 15, 2019 |
Contact name |
eunmi Park |
E-mail(s) |
eunmi_park@dfci.harvard.edu
|
Organization name |
Dana-Farber Cancer Institute
|
Street address |
44 Binney street
|
City |
BOSTON |
State/province |
MA |
ZIP/Postal code |
02210 |
Country |
USA |
|
|
Platform ID |
GPL11154 |
Series (1) |
GSE46902 |
FANCD2 Activates Transcription of TAp63 and Suppresses Tumorigenesis |
|
Relations |
SRA |
SRX277586 |
BioSample |
SAMN02143979 |