NCBI Logo
GEO Logo
   NCBI > GEO > Accession DisplayHelp Not logged in | LoginHelp
GEO help: Mouse over screen elements for information.
          Go
Sample GSM1048273 Query DataSets for GSM1048273
Status Public on Dec 06, 2012
Title crol-F7-16_SOLEXA_2.5
Sample type SRA
 
Source name synthetic library
Organism synthetic construct
Characteristics library: ZFP library
library selection: bacterial one-hybrid (B1H) selected
Treatment protocol refer to Enuameh MS et al. 2012 [PMID 22689783]
Growth protocol refer to Enuameh MS et al. 2012 [PMID 22689783]
Extracted molecule other
Extraction protocol Following each selection, all of the cells were scraped off the plate. The randomized portion of the prey vector containing the selected transcription factor binding sites were extracted and amplified using PCR.
The PCR products from different experiments were digested with different restriction enzymes in the first step of uniquely encoding sequences from different experiments. The restriction enzyme fragments were then barcoded, pooled and sequenced using a Illumina Genome Analyzer IIx or Illumina HiSeq 2000 machine as indicated in Gupta et al. (2011). Nucleic Acids Res. 39(1): 381–392. A more detailed description of the selection conditions employed for each zinc finger cluster is given in the methods section of this publication as well as the supplemental material of Noyes et al. (2008). Cell. 133(7):1277-1289.
 
Library strategy OTHER
Library source other
Library selection other
Instrument model Illumina HiSeq 2000
 
Description molecule: plasmid DNA
Sample 34
Data processing The extracted sequences from the Illumina data were submitted to MEME for analysis. The parameters used as follows: Motif width was set at 5 to 15, the distribution of motif set as zoops, while allowing sites on + or - DNA strands. All other parameters were at the default settings. Aligned sequences were subsequently extracted from the MEME results and output in fasta format.
Supplementary_files_format_and_content: fasta and contains aligned extracted binding site sequences along with 'sequence rank.number' For example, '457.1' represent the corresponding unique sequence is ranked 457th and is 1 in number.
Supplementary_files_format_and_content: In the file name, e.g. CG3407_SOLEXA_2.5.fa, CG3407 refers to Gene name, SOLEXA denotes the sequencing method and 2.5 is the inhibitor (3-AT) concentration used in the Bacterial One-Hybrid selection.
 
Submission date Dec 04, 2012
Last update date May 15, 2019
Contact name Scot Wolfe
E-mail(s) [email protected]
Organization name UMass Medical School
Department MCCB
Street address 364 Plantation Street, LRB 619
City Worcester
State/province MA
ZIP/Postal code 01605
Country USA
 
Platform ID GPL15228
Series (1)
GSE42709 Global analysis of Drosophila Cys2-His2 zinc finger proteins reveals a multitude of novel recognition motifs and binding determinants.
Relations
SRA SRX208256
BioSample SAMN01822854

Supplementary file Size Download File type/resource
GSM1048273_crol_F7-16_SOLEXA_2.5.fa.gz 19.0 Kb (ftp)(http) FA
SRA Run SelectorHelp
Raw data are available in SRA
Processed data provided as supplementary file

| NLM | NIH | GEO Help | Disclaimer | Accessibility |
NCBI Home NCBI Search NCBI SiteMap