|
Status |
Public on Sep 16, 2023 |
Title |
ChIP_Anti_MucR_Ba2308_WT_rep1 |
Sample type |
SRA |
|
|
Source name |
Bacterial
|
Organism |
Brucella abortus 2308 |
Characteristics |
cell type: Bacterial genotype: wild type treatment: Cells were growing in LB, fixed by 3% formaldehyde for 30min at room temperature antibody: ChIP using anti-MucR antibodies
|
Extracted molecule |
genomic DNA |
Extraction protocol |
Wild type and mutant cells of Brucella abortus 2308 growing in LB were crosslinked using 3% formaldehyde and then lysed by treatment of lysosome and 1% SDS as previouly discribed (Wang et al 2015). Standard library construction protocol was used for Illumina Nextseq500 sequencing platforms. Illumina Truseq indexes were used.
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|
|
Library strategy |
ChIP-Seq |
Library source |
genomic |
Library selection |
ChIP |
Instrument model |
Illumina NextSeq 500 |
|
|
Data processing |
Reads from each end of a DNA fragment were represented in each of the two FASTQ files generated by Illumina paired-end sequencing. The sequencing reads were mapped to the combined B. abortus 2308 (NCBI Reference Sequence GCA_000054005.1) by the hiclib pipline. Assembly: B. abortus 2308 (NCBI Reference Sequence GCA_000054005.1) Supplementary files format and content: Files ending with .matrix.txt: tab-delimited text files of the iteratively-corrected Hi-C contact maps/matrices. Files ending with .csv files are comma-separated values files of ChIP-seq/WGS results.
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|
|
Submission date |
Jun 14, 2023 |
Last update date |
Sep 16, 2023 |
Contact name |
Xindan Wang |
E-mail(s) |
xindan@iu.edu
|
Organization name |
Indiana University at Bloomington
|
Department |
Biology
|
Lab |
Biology Building 225
|
Street address |
1001 E 3rd St
|
City |
Bloomington |
State/province |
IN |
ZIP/Postal code |
47405 |
Country |
USA |
|
|
Platform ID |
GPL33491 |
Series (1) |
GSE234935 |
Brucella MucR acts as an H-NS-like protein to silence virulence genes and structure the nucleoid  |
|
Relations |
BioSample |
SAMN35737118 |
SRA |
SRX20681639 |