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Series GSE60200 Query DataSets for GSE60200
Status Public on Mar 01, 2015
Title Quantitative modeling of transcription factor binding specificities using DNA shape
Organism Homo sapiens
Experiment type Genome binding/occupancy profiling by high throughput sequencing
Summary The SELEX-seq platform was used to generate DNA-binding affinity predictions for the human Max transcription factor. This experiment was performed as part of a cross-validation study comparing the accuracy of DNA shape-augmented TF binding specificity models across two different platforms (SELEX-seq and gcPBM)
 
Overall design Two rounds of SELEX were performed on Max protein as described in Slattery et al, Cell, 2011 (PMID 22153072). Briefly, His-tagged Max was incubated with a randomized 16mer oligonucleotide library (GTTCAGAGTTCTACAGTCCGACGATCTGG[ACGT]{16}CCAGAACTCGTATGCCGTCTTCTGCTTG). Max bound DNA was amplified and sequenced as described (Slattery et al, 2011).
 
Contributor(s) Mann RS, Bussemaker HJ, Gordân R
Citation(s) 25775564
Submission date Aug 07, 2014
Last update date May 15, 2019
Contact name Namiko Abe
E-mail(s) abenamiko@gmail.com
Phone 212-305-2111
Organization name Columbia University
Department Biochemistry and Molecular Biophysics
Lab Richard Mann
Street address 701 W. 168th St HHSC1104
City New York
State/province NY
ZIP/Postal code 10032
Country USA
 
Platforms (1)
GPL16791 Illumina HiSeq 2500 (Homo sapiens)
Samples (1)
GSM1467529 Human Max protein
Relations
BioProject PRJNA257744
SRA SRP045333

Download family Format
SOFT formatted family file(s) SOFTHelp
MINiML formatted family file(s) MINiMLHelp
Series Matrix File(s) TXTHelp

Supplementary file Size Download File type/resource
GSE60200_Max_selex_normalized.txt.gz 251.8 Kb (ftp)(http) TXT
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Raw data are available in SRA
Processed data are available on Series record

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