|
Status |
Public on Mar 13, 2020 |
Title |
ChIP-seq_Col-0_air_H3K4me3 |
Sample type |
SRA |
|
|
Source name |
histone modification
|
Organism |
Arabidopsis thaliana |
Characteristics |
tissue: etiolated seedlings genotype: Col-0 antibodies: H3K4me3 (EMD Millipore, 04-745)
|
Treatment protocol |
no treatment or 4 hours of JA treatment
|
Growth protocol |
etiolated seedlings
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Kaufmann et al. 2010 DOI:10.1038/nprot.2009.244 Libraries were prepared for sequencing using standard Illumina protocols
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina HiSeq 2500 |
|
|
Description |
Sample 2 Wig file contains: SICER comparison Sample 2 vs Sample 2
|
Data processing |
base-calling using RTA 2.7.7 alignment using Bowtie2 2.1.0 bam file comparison using deepTools2.0/bamCompare data extraction using bigWigAverageOverBed ChIP-seq peak identification with SICER 1.1 with the following setting: redundancy threshold (1), window size (200), fragment size (100), effective genome fraction (0.8), gap size (600), FDR (0.01) Genome_build: TAIR10 Supplementary_files_format_and_content: wig files with SICER output
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|
|
Submission date |
Jun 27, 2019 |
Last update date |
Mar 14, 2020 |
Contact name |
Joseph R Ecker |
E-mail(s) |
ecker@salk.edu
|
Phone |
8584534100
|
Organization name |
HHMI-Salk-Institute
|
Department |
Genomic Analysis Laboratory
|
Lab |
Ecker lab
|
Street address |
10010 North Torrey Pines Road
|
City |
La Jolla |
State/province |
CA |
ZIP/Postal code |
92037 |
Country |
USA |
|
|
Platform ID |
GPL17639 |
Series (1) |
GSE133408 |
The jasmonate-response genome regulatory program is defined by the direct targets of transcription factors MYC2 and MYC3, chromatin modification and gene expression changes |
|
Relations |
BioSample |
SAMN12147612 |
SRA |
SRX6370134 |